| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs15564 | snp | A/C | 0.496842 | 0.0396107 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:627854 | GGCCCGGCTTGTTTC[A/C]GACCAAGATTCCCGG | 57799 |
| rs763011 | snp | C/T | 0.43221 | 0.171171 | intron-variant | RAB40C | GRCh38.p7 | 16:623277 | AAAAGTTACCCCTCT[C/T]CAGCCTTTTAGCATT | 57799 |
| rs763012 | snp | C/T | 0.432357 | 0.171014 | intron-variant | RAB40C | GRCh38.p7 | 16:624024 | GGCCAGCATGCACGC[C/T]TTTACATGCACTGCT | 57799 |
| rs763013 | snp | C/T | 0.432357 | 0.171014 | intron-variant | RAB40C | GRCh38.p7 | 16:624029 | GCATGCACGCTTTTA[C/T]ATGCACTGCTGCTGT | 57799 |
| rs763014 | snp | C/T | 0.495596 | 0.0467178 | intron-variant | RAB40C | GRCh38.p7 | 16:625680 | CTGTGCACACGACAG[C/T]CGGGCGTGGAGCCCA | 57799 |
| rs763015 | snp | C/G | 0.281841 | 0.247964 | intron-variant | RAB40C | GRCh38.p7 | 16:626261 | AGGGGCTCGGCCGGC[C/G]GCAGGTCAGTGACTT | 57799 |
| rs1894675 | snp | C/G | 0.326035 | 0.238157 | | | GRCh38.p7 | 16:596865 | TTGAGCCTAAGGTAG[C/G]GAGGAGGCTTCTGAG | 57799 |
| rs1984395 | snp | C/T | 0.464841 | 0.127841 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628843 | ACGACATGGCCAGCA[C/T]GCAGAAGGAGCCCTC | 57799 |
| rs2269556 | snp | A/G | 0.464629 | 0.128197 | intron-variant | RAB40C | GRCh38.p7 | 16:625215 | GACACCATGGAAGGC[A/G]CCCACCCCCCTGCTG | 57799 |
| rs2269557 | snp | C/T | 0.433463 | 0.169827 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:627629 | ATCTCCTAGCGGGGA[C/T]GGGCGGGGCCGCCTG | 57799 |
| rs2384972 | snp | C/T | 0.495891 | 0.0451408 | intron-variant | RAB40C | GRCh38.p7 | 16:624424 | AGGAAGGACACCTCT[C/T]GCTGAGGGAGACCCT | 57799 |
| rs2384973 | snp | A/G | 0.256619 | 0.249912 | intron-variant | RAB40C | GRCh38.p7 | 16:603739 | gctttctgggaggag[A/G]gtggatgtgctcctg | 57799 |
| rs2384974 | snp | C/G | 0.497695 | 0.0338674 | intron-variant | RAB40C | GRCh38.p7 | 16:601279 | AATTCAGAAAGGATG[C/G]ACACTTTCAGAATGA | 57799 |
| rs2384975 | snp | A/C | 0.497695 | 0.0338674 | intron-variant | RAB40C | GRCh38.p7 | 16:601115 | ACACAAGCAGCAGGC[A/C]CATTTACTGAACGGT | 57799 |
| rs2384976 | snp | A/G | 0.25634 | 0.24992 | intron-variant | RAB40C | GRCh38.p7 | 16:601113 | ACAAGCAGCAGGCCC[A/G]TTTACTGAACGGTGA | 57799 |
| rs2891650 | snp | C/T | 0.431473 | 0.171952 | intron-variant | RAB40C | GRCh38.p7 | 16:598547 | TGTGAGACAGAGTCT[C/T]GCTCTGTCACCAAGC | 57799 |
| rs3180836 | snp | A/C | | | utr-variant-3-prime, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629268 | TAATTCAGCTGTGGT[A/C]CCCACGTTTTGCTGT | 57799 |
| rs3838961 | in-del | -/G | 0.439502 | 0.163061 | intron-variant | RAB40C | GRCh38.p7 | 16:617629 | AGGAGGATCACCTGA[-/G]GTCAGGAGTCCAAGA | 57799 |
| rs3838962 | in-del | -/C | 0.430269 | 0.173214 | intron-variant | RAB40C | GRCh38.p7 | 16:625088 | GACTGGCCGAGAGGA[-/C]ACTTAGCTTCCACAG | 57799 |
| rs4144003 | snp | C/T | 0.498852 | 0.0239341 | intron-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595968 | AGGAAACTGTTGAGT[C/T]AGTAGGTAGAATATT | 57799 |
| rs4247097 | snp | A/G | 0.497586 | 0.0346604 | intron-variant | RAB40C | GRCh38.p7 | 16:604224 | CACACCCGGCTCAGA[A/G]CTAGTTCTTTTAAAT | 57799 |
| rs4984670 | snp | A/G | 0.497329 | 0.0364438 | intron-variant | RAB40C | GRCh38.p7 | 16:591044 | ATCTGGGGTCCGAGG[A/G]AAGGTGTCATAGATC | 57799 |
| rs4984671 | snp | C/T | 0.433236 | 0.170072 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594860 | AGTCTTACTCTCTTG[C/T]GCAGGCTGGAGTGCA | 57799 |
| rs4984672 | snp | A/G | 0.464203 | 0.128908 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596421 | AAGGGGTTGCATCAC[A/G]GCTGAGTCCTCCCCT | 57799 |
| rs4984673 | snp | A/G | 0.428937 | 0.17459 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596571 | CATCCTGGTGCGGAG[A/G]ACGCTGCCGAACCAC | 57799 |
| rs4984674 | snp | A/C | 0.117188 | 0.211804 | intron-variant | RAB40C | GRCh38.p7 | 16:599709 | TCGCAAGGTTTTGTT[A/C]CCTCGTGGCATCAGT | 57799 |
| rs4984675 | snp | C/T | 0.489893 | 0.0703642 | intron-variant | RAB40C | GRCh38.p7 | 16:620117 | AAGAGGAGTTGGGGC[C/T]GGTGCGGTGGTTCAC | 57799 |
| rs4984676 | snp | A/G | 0.497151 | 0.037632 | intron-variant | RAB40C | GRCh38.p7 | 16:620168 | GGGAGGCCAAGGCAG[A/G]CAGATCACGAGGTCA | 57799 |
| rs4984677 | snp | A/G | 0.495818 | 0.0455352 | intron-variant | RAB40C | GRCh38.p7 | 16:621682 | GGGTCACCCAGGTGC[A/G]GGTCCCTTGGTGTGT | 57799 |
| rs4984678 | snp | A/G | 0.432504 | 0.170857 | intron-variant | RAB40C | GRCh38.p7 | 16:624737 | GGACGTTGGGGAGAG[A/G]CGGGCATAGGGGAAT | 57799 |
| rs4984898 | snp | G/T | 0.497091 | 0.0380279 | intron-variant | RAB40C | GRCh38.p7 | 16:591164 | GTGTCATGGGTCTGG[G/T]ATCTCAGGGGAAGGT | 57799 |
| rs4984899 | snp | C/T | 0.427423 | 0.176128 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594048 | CCCCCAGGAACCACC[C/T]GCACAGGGTGCACAC | 57799 |
| rs4984900 | snp | A/G | 0.426813 | 0.17674 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:597006 | TAGCGGAGGGACAAG[A/G]GCATTGGCGCTGTGG | 57799 |
| rs4984901 | snp | A/G | 0.497271 | 0.0368399 | intron-variant | RAB40C | GRCh38.p7 | 16:602623 | tttttagtagagatg[A/G]ggtttcaccatgtcg | 57799 |
| rs4984902 | snp | G/T | 0.429388 | 0.174127 | intron-variant | RAB40C | GRCh38.p7 | 16:605262 | agcagccccattgtt[G/T]catagtcccatcagc | 57799 |
| rs5815051 | in-del | -/T | 0.485392 | 0.0842056 | intron-variant | RAB40C | GRCh38.p7 | 16:604239 | GCTAGTTCTTTTAAA[-/T]TTTTTTTTTTTAATT | 57799 |
| rs7185390 | snp | A/G | 0.490231 | 0.0692021 | intron-variant | RAB40C | GRCh38.p7 | 16:616382 | tGAGTActgtcaccc[A/G]ggcaggagtgcagtg | 57799 |
| rs7185527 | snp | C/T | 0.256619 | 0.249912 | intron-variant | RAB40C | GRCh38.p7 | 16:600708 | AGTGAGCCGAGTTTG[C/T]ACCACTACACTCCAG | 57799 |
| rs7189914 | snp | C/T | 0.257732 | 0.24988 | intron-variant | RAB40C | GRCh38.p7 | 16:592222 | GTCCTGTCTGACTGC[C/T]CTGAGCGTCTGCTAT | 57799 |
| rs7190358 | snp | A/G | 0.253544 | 0.249975 | intron-variant | RAB40C | GRCh38.p7 | 16:600788 | TTGGTGCCTACGTGC[A/G]TCACACAGACAGTTT | 57799 |
| rs7191397 | snp | G/T | 0.497445 | 0.0356514 | intron-variant | RAB40C | GRCh38.p7 | 16:616517 | ctaattttttgtatt[G/T]ttagtagagacgggg | 57799 |
| rs7191584 | snp | C/T | 0.430136 | 0.173352 | intron-variant | RAB40C | GRCh38.p7 | 16:601517 | TCCCCGCCGCAGCCG[C/T]GTCAGCAGAGCAATG | 57799 |
| rs7197889 | snp | A/G | 0.103438 | 0.202533 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596388 | GTCTGGAGCCCCTGC[A/G]AGCTGGCGTAGAGCA | 57799 |
| rs7198207 | snp | C/T | 0.256061 | 0.249927 | intron-variant | RAB40C | GRCh38.p7 | 16:598515 | gcagagagctgagat[C/T]gtgccactgcactcc | 57799 |
| rs7198877 | snp | A/G | 0.496681 | 0.0405994 | intron-variant | RAB40C | GRCh38.p7 | 16:611439 | TCTCAGGTCAGCCTC[A/G]TGGGGGCTTCAACAG | 57799 |
| rs7198884 | snp | A/G | 0.431916 | 0.171483 | intron-variant | RAB40C | GRCh38.p7 | 16:611451 | CTCATGGGGGCTTCA[A/G]CAGCCAGGACCAAAA | 57799 |
| rs7199115 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | RAB40C | GRCh38.p7 | 16:616320 | GGTCAGTCCAGAGTC[C/T]GGAGAAGCAGCATtt | 57799 |
| rs7203005 | snp | A/G | 0.104504 | 0.2033 | intron-variant | RAB40C | GRCh38.p7 | 16:609852 | GGCTCAGGATGGAGG[A/G]CGGGAGCTGTGTGCC | 57799 |
| rs7203694 | snp | A/G | 0.25634 | 0.24992 | intron-variant | RAB40C | GRCh38.p7 | 16:602941 | TTGTAATCATTGAAA[A/G]TAATCTGAGAGCTAT | 57799 |
| rs7204088 | snp | C/T | 0.432063 | 0.171327 | intron-variant | RAB40C | GRCh38.p7 | 16:611142 | TCCCAGAGCAGCCTC[C/T]GATTCAAGAGCAAGG | 57799 |
| rs7204439 | snp | C/T | 0.492435 | 0.0610346 | intron-variant | RAB40C | GRCh38.p7 | 16:611335 | GGTGTTGCTGGCGCC[C/T]GCCTGCTTGGCCACA | 57799 |
| rs7205409 | snp | C/T | 0.478354 | 0.101757 | intron-variant | RAB40C | GRCh38.p7 | 16:592610 | TGGTGGGCGGCCAAG[C/T]TGATTGTGAAGGTGG | 57799 |
| rs7500178 | snp | A/G | 0 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:605088 | ttagcctggtgtggt[A/G]acgcacacttgtaat | 57799 |
| rs8047461 | snp | A/G | 0.261884 | 0.249717 | intron-variant | RAB40C | GRCh38.p7 | 16:591260 | CATCTGGGGTCTGAG[A/G]GAAGGTGTCATAGAT | 57799 |
| rs8050792 | snp | C/T | 0.497359 | 0.0362457 | intron-variant | RAB40C | GRCh38.p7 | 16:606033 | ATTTTTAGTTTGGAT[C/T]CAGTTTATTTATAAT | 57799 |
| rs8054842 | snp | C/T | 0.495095 | 0.0492773 | intron-variant | RAB40C | GRCh38.p7 | 16:622799 | GTGAGCCACGGCGCC[C/T]GGCCGAAGTCGCTAG | 57799 |
| rs8055671 | snp | C/T | 0.254664 | 0.249956 | intron-variant | RAB40C | GRCh38.p7 | 16:609469 | TCAGCCCAAAAGAAG[C/T]GGCCACGAGACGCCG | 57799 |
| rs8063979 | snp | A/G | 0.256619 | 0.249912 | intron-variant | RAB40C | GRCh38.p7 | 16:609543 | TAGGGTCTGTCCTTG[A/G]GGGTCACCAGAATGT | 57799 |
| rs9673269 | snp | A/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:613098 | CGCCCTGGCCTGTAG[A/C]ATCAAGAGCAAGGGA | 57799 |
| rs9673273 | snp | A/G | 0.259397 | 0.249823 | intron-variant | RAB40C | GRCh38.p7 | 16:613193 | GGGACAGCCGCCCTC[A/G]CCTGTAGAATCAGCA | 57799 |
| rs9673790 | snp | C/G/T | 0.00279162 | 0.0372561 | intron-variant | RAB40C | GRCh38.p7 | 16:613054 | AGGGACAGCCGCCCT[C/G/T]GCCTGTAGCATCAAG | 57799 |
| rs9674305 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RAB40C | GRCh38.p7 | 16:613052 | GCAGGGACAGCCGCC[C/T]TGGCCTGTAGCATCA | 57799 |
| rs9674306 | snp | A/C | 0 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:613063 | CGCCCTGGCCTGTAG[A/C]ATCAAGAGCAAGGGA | 57799 |
| rs9745918 | snp | G/T | 0.496999 | 0.0386216 | intron-variant | RAB40C | GRCh38.p7 | 16:614196 | ACTCTACCGCATCCC[G/T]ATGGTGAACTGCTAA | 57799 |
| rs9923727 | snp | G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:602601 | gcccggctagttttt[G/T]ggtatttttttagta | 57799 |
| rs9929621 | snp | C/T | 0.284995 | 0.247539 | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629412 | CGGGCTGACCTGCCG[C/T]GGTTGGCTGGGTTCG | 57799 |
| rs9932481 | snp | A/G | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:606473 | GTGTGGGTTTCCCTG[A/G]GCTGAAGTCAAGGTG | 57799 |
| rs9932507 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | RAB40C | GRCh38.p7 | 16:623200 | CGGGCCTTCTGCTCT[A/C]TTTCTAGAGTTTTCA | 57799 |
| rs9935061 | snp | G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:606527 | gtcctcagtccagtg[G/T]gggtttccctgggct | 57799 |
| rs10153107 | snp | C/T | 0.0611083 | 0.163768 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628877 | GGACCCAGGACCCCC[C/T]GTGGTGGACTCCGCG | 57799 |
| rs10153225 | snp | A/G | 0.0596104 | 0.162024 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628980 | TGGGAGATGAGGGCC[A/G]TGGCCTGCATGAACT | 57799 |
| rs10656981 | in-del | -/AT/TA | | | intron-variant | RAB40C | GRCh38.p7 | 16:600441 | GTTTAAAACATTGTT[-/AT/TA]GTTGGACTTTTTTAA | 57799 |
| rs11248939 | snp | A/G | 0.167158 | 0.235875 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:597094 | GGGTGCTGCACATGT[A/G]GGTAGCAGGGGGAGG | 57799 |
| rs11248940 | snp | C/T | 0.19646 | 0.2442 | intron-variant | RAB40C | GRCh38.p7 | 16:605686 | AAGGCTGCAGTGCAT[C/T]GGCTCCACTCCAGAT | 57799 |
| rs11248941 | snp | G/T | 0.236724 | 0.249647 | intron-variant | RAB40C | GRCh38.p7 | 16:608271 | agaactcactcaccc[G/T]cacaaaaacagcagg | 57799 |
| rs11285441 | in-del | -/C | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:611869 | GTAGAATCAAGAGCA[-/C]GGGACAGCCGCCCTG | 57799 |
| rs11340032 | snp | A/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:612487 | GTAGAATCAAGAGCA[A/C]GGGACAGCCGCCCTG | 57799 |
| rs11548187 | snp | A/C/T | 3.5092e-05 | 0.00418865 | synonymous-codon, missense | RAB40C | GRCh38.p7 | 16:627599 | CCCCAGAACTGCTCG[A/C/T]GGAGTAACTGCAAGA | 57799 |
| rs11548188 | snp | A/G | 0.278399 | 0.248382 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628020 | TGACTTCATGGCCAC[A/G]CCAGCTGCGGGGACG | 57799 |
| rs11548189 | snp | C/G | 0.0596104 | 0.162024 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628264 | AGGAGGTGCACCTGG[C/G]AGCCCACATTTTTGT | 57799 |
| rs11639703 | snp | A/G | 0.187369 | 0.242028 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594393 | ATCACGGTTTGCTGT[A/G]GATGTTGGGGCCTGG | 57799 |
| rs11639717 | snp | C/T | 0.308908 | 0.242961 | intron-variant | RAB40C | GRCh38.p7 | 16:626989 | ATGAGTCAGGACGCG[C/T]GCTCCCCCGCTCTAG | 57799 |
| rs11639978 | snp | A/G | 0.190833 | 0.242898 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:589042 | GACGAGGGCTCGGCG[A/G]CGCCCCCGGGAAGAG | 57799 |
| rs11641903 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | RAB40C | GRCh38.p7 | 16:605648 | CTCCCTCCTTCCCCG[C/T]GCCGAGTGGTCTCCC | 57799 |
| rs11642273 | snp | A/G | 0.255224 | 0.249945 | intron-variant | RAB40C | GRCh38.p7 | 16:601538 | CAGAGCAATGTGATC[A/G]TTGCTGGGACTGTTC | 57799 |
| rs11643412 | snp | A/G | 0.261056 | 0.249755 | intron-variant | RAB40C | GRCh38.p7 | 16:615323 | AGGCAGAGAGACCGC[A/G]TGGCTGGCTTGCAGG | 57799 |
| rs11645708 | snp | C/T | 0.259674 | 0.249813 | intron-variant | RAB40C | GRCh38.p7 | 16:611080 | GTGGGCAACCGGGTG[C/T]GGAGCCTGCAGGATG | 57799 |
| rs11647220 | snp | C/T | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594825 | TCGTCTTCCtttttt[C/T]tttttttttttttag | 57799 |
| rs11648607 | snp | A/G | 0.256897 | 0.249905 | intron-variant | RAB40C | GRCh38.p7 | 16:621245 | CACCCCGGGAGCCCA[A/G]CCCTGTCCTGTGTCT | 57799 |
| rs11649661 | snp | C/T | 0.169435 | 0.236663 | intron-variant | RAB40C | GRCh38.p7 | 16:591486 | TAGGCACGCTGTTCC[C/T]CTGAGGTATTTGCTT | 57799 |
| rs11861429 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | RAB40C | GRCh38.p7 | 16:621502 | ACTCCCCGCTGCCGT[C/T]ACCTGTCACACAGCA | 57799 |
| rs11861544 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596503 | GGGCCACGTCAGCCA[C/G]GGTGTCATCCGCCGG | 57799 |
| rs11863012 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RAB40C | GRCh38.p7 | 16:621369 | AGACACAGACTAGCA[A/G]GGACTGTCTGTCCCA | 57799 |
| rs12149200 | snp | C/T | 0.0383715 | 0.133092 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628430 | ATACTTGATGGGCAG[C/T]GGTGCAGACCCCGGG | 57799 |
| rs12149324 | snp | C/G | 0.261608 | 0.24973 | intron-variant | RAB40C | GRCh38.p7 | 16:606997 | GCCGGCCCAGACAGA[C/G]AGACTACCACCTGAG | 57799 |
| rs12149951 | snp | G/T | 0.261608 | 0.24973 | intron-variant | RAB40C | GRCh38.p7 | 16:606842 | cttatgtagttaatt[G/T]gccccacccagataa | 57799 |
| rs12149958 | snp | A/G | 0.258843 | 0.249844 | intron-variant | RAB40C | GRCh38.p7 | 16:606985 | TGCTGGTGGCAGGCC[A/G]GCCCAGACAGACAGA | 57799 |
| rs12444525 | snp | A/G | 0.407158 | 0.194426 | intron-variant | RAB40C | GRCh38.p7 | 16:623430 | cgaggtgggcagatc[A/G]ggaggtcaggagatc | 57799 |
| rs12446884 | snp | A/C | 0.167484 | 0.23599 | intron-variant | RAB40C | GRCh38.p7 | 16:623577 | gagaatggcgtgaac[A/C]cggaagcggagatcg | 57799 |
| rs12447387 | snp | A/G | 0.26818 | 0.249338 | intron-variant | RAB40C | GRCh38.p7 | 16:617490 | CCTCCTGCCCCGGAA[A/G]ACCTGATTCCGTGGT | 57799 |
| rs12447410 | snp | A/G | 0.256619 | 0.249912 | intron-variant | RAB40C | GRCh38.p7 | 16:617513 | TCCGTGGTGGCTGTG[A/G]GCCCCTTCCCTCCCC | 57799 |
| rs12447820 | snp | G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:599952 | GATTCGCAAGGTTTT[G/T]TTCCCTCGTGGCATC | 57799 |
| rs12596770 | snp | C/T | 0.160609 | 0.233472 | intron-variant | RAB40C | GRCh38.p7 | 16:615732 | TTTGGGAGGCCAAGG[C/T]GGGCGAATCACCTGA | 57799 |
| rs12600216 | snp | A/G | 0.21875 | 0.248039 | intron-variant | RAB40C | GRCh38.p7 | 16:606434 | GGTGTTGGCTGACAC[A/G]CAGTCCTCTCGGTCC | 57799 |
| rs12919894 | snp | A/G | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:606302 | GGTGTTGGCTGACAC[A/G]CAGTCCTCTCGGTCC | 57799 |
| rs12920965 | snp | G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:617662 | agcctggccaacatg[G/T]tgaaacgccatctct | 57799 |
| rs12920971 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:617669 | ccaacatggtgaaac[C/G]ccatctctactaaaa | 57799 |
| rs12921112 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:617716 | ggtgtggtggcgggc[A/G]cctgtagtcccagcc | 57799 |
| rs12921119 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:617723 | tggcgggcgcctgta[A/G]tcccagccactcagg | 57799 |
| rs12921145 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:617785 | gaggcagaagttgca[A/G]tgagctgagattgca | 57799 |
| rs12922012 | snp | C/G/T | 0.495999 | 0.0445491 | intron-variant | RAB40C | GRCh38.p7 | 16:607552 | ctcacgcctgtaatc[C/G/T]cagcactttgggagg | 57799 |
| rs12924371 | snp | A/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:617646 | tcaggagtccaagac[A/C]agcctggccaacatg | 57799 |
| rs12924517 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:617736 | tagtcccagccactc[A/G]ggaggctgaggcagt | 57799 |
| rs12924543 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:617778 | aacccgggaggcaga[A/G]gttgcagtgagctga | 57799 |
| rs12929823 | snp | A/G | 0.496778 | 0.0400063 | intron-variant | RAB40C | GRCh38.p7 | 16:611665 | TAGAATCAAGAGCAG[A/G]GACAGCCGCCCTGGC | 57799 |
| rs12932411 | snp | A/C | 0.437259 | 0.165632 | intron-variant | RAB40C | GRCh38.p7 | 16:615811 | TACTAAAATTATAAA[A/C]ATTAGCCGGCTGTGG | 57799 |
| rs12934493 | snp | A/T | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:611756 | GCCCTGGCCTGTAGA[A/T]TCAAGAGCAGGGACA | 57799 |
| rs12935215 | snp | C/T | 0.495708 | 0.0461266 | intron-variant | RAB40C | GRCh38.p7 | 16:620605 | CCTGACAGGCTCCAC[C/T]GCGGGCATCCCAGCC | 57799 |
| rs12935332 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:617639 | cctgaggtcaggagt[C/T]caagacaagcctggc | 57799 |
| rs12935343 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:617676 | ggtgaaacgccatct[C/T]tactaaaaatacaaa | 57799 |
| rs12935490 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:617731 | gcctgtagtcccagc[C/T]actcaggaggctgag | 57799 |
| rs17138458 | snp | A/G | 0.0356815 | 0.128715 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593873 | AACAGAGCGCTTTGC[A/G]TAGAGTGCCCCTGGG | 57799 |
| rs17138487 | snp | A/G | 0.0360663 | 0.129354 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594438 | TCTGTGGGGCCACAC[A/G]CTGCCTGCTGTACCC | 57799 |
| rs17138503 | snp | C/T | 0.0232847 | 0.105357 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595201 | AGCTAATGCTGCCAG[C/T]GTGTGATGAGTGTTG | 57799 |
| rs17138547 | snp | C/T | 0.0941369 | 0.195465 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596639 | GACTTCCTGGGCGGT[C/T]GGGAGAAGGATGTGC | 57799 |
| rs17555255 | snp | G/T | 0.0115144 | 0.0749975 | utr-variant-3-prime, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629241 | TCCGAACCGTTCTTT[G/T]TACAGTAAATGTAAT | 57799 |
| rs28418424 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:598581 | AAAAAAAAAAAAAAA[A/G]AAAAAAGAAAATTAG | 57799 |
| rs28483242 | snp | A/C | 0.0596104 | 0.162024 | intron-variant | RAB40C | GRCh38.p7 | 16:625617 | CTCCTGTGGCCCCGG[A/C]TCTGCACCCTGCACT | 57799 |
| rs28523441 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:620765 | ATCCCAGCCCCCCGC[C/T]GACGGGCTCCACCGC | 57799 |
| rs28607551 | snp | A/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:598746 | ACCCTGTCTCAAAAA[A/T]TAAAAAATAAAGAAA | 57799 |
| rs28618284 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:598587 | AAAAAAAAAGAAAAA[A/G]GAAAATTAGCTGGGT | 57799 |
| rs28649814 | snp | A/G | | | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628847 | CATGGCCAGCACGCA[A/G]AAGGAGCCCTCCCGG | 57799 |
| rs28723552 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:621566 | CGTGCCGCCGAAGGC[C/G]GGGCTCCCTAGACTT | 57799 |
| rs28766574 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | RAB40C | GRCh38.p7 | 16:620853 | GACGGGCTCCACCGC[A/G]GGCATCCCAGCTCCC | 57799 |
| rs34011309 | snp | A/G | 0.49706 | 0.0382258 | intron-variant | RAB40C | GRCh38.p7 | 16:618443 | CACCCAGGCTGGAGT[A/G]CAGTGGCACAGTCTC | 57799 |
| rs34045961 | in-del | -/C | | | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:597738 | AAGCAATCCGCCCGC[-/C]TCAGCTTCCCAAAGT | 57799 |
| rs34274490 | in-del | -/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:622929 | GGTGCCGTTCGTTAG[-/G]CGGCTGCTGGTCACC | 57799 |
| rs34353619 | in-del | -/G | | | utr-variant-5-prime, upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:589502 | CCGCGCGTTGAAGGG[-/G]CGGATACAAACAACG | 57799 |
| rs34408623 | in-del | -/C | 0.256061 | 0.249927 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594824 | TCGTCTTCCTTTTTT[-/C]TTTTTTTTTTTTTTA | 57799 |
| rs34498660 | snp | A/G | 0.497271 | 0.0368399 | intron-variant | RAB40C | GRCh38.p7 | 16:616149 | GTAGTTCAGCTACTC[A/G]GCAGGCTGAGGCTAG | 57799 |
| rs34511663 | in-del | -/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:603757 | CCTCCCAGAAAGCCC[-/C]TCAGGCCCTGCCGAG | 57799 |
| rs34641498 | in-del | -/T | | | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596686 | GGTGTCAGGGACCAG[-/T]AAGTTACGAAGGCGG | 57799 |
| rs34678985 | snp | A/G | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:612980 | AGAGCAGGGACAGCC[A/G]CCCTGGCCTGTAGAA | 57799 |
| rs34768407 | in-del | -/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:626385 | TGCCATGCCTGTGGG[-/G]TCCCTGGCATTGCTG | 57799 |
| rs34812060 | snp | A/G | 0.43598 | 0.167067 | intron-variant | RAB40C | GRCh38.p7 | 16:614802 | ACTCTACCTCGTCCC[A/G]ACGGTGAACTGCCAA | 57799 |
| rs34836597 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RAB40C | GRCh38.p7 | 16:599631 | AGGTTTTGTTACCTC[A/G]TGGCATTAATCAGCG | 57799 |
| rs34895008 | in-del | -/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:621095 | GAGCTGTCATTTTCC[-/C]ACATGCGAGGAGCAG | 57799 |
| rs34997977 | snp | G/T | 0.46014 | 0.13543 | intron-variant | RAB40C | GRCh38.p7 | 16:627020 | GGGATGAGTCAGGAC[G/T]CTTGAAGGGCCAGAT | 57799 |
| rs35026625 | snp | C/G | 0.117886 | 0.21224 | intron-variant | RAB40C | GRCh38.p7 | 16:622361 | CAGCGCCAAGTGCCT[C/G]CACCCCCTTGACCCC | 57799 |
| rs35033757 | in-del | -/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:590812 | TGTCATGGGTCTAGG[-/C]ATCATCTGGGGTCCG | 57799 |
| rs35049796 | in-del | -/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:624412 | CTCTGGCCTCGAAGG[-/G]TCTCCCTCAGCAAGA | 57799 |
| rs35067229 | snp | C/T | 0.497241 | 0.037038 | intron-variant | RAB40C | GRCh38.p7 | 16:599638 | GTTACCTCGTGGCAT[C/T]AATCAGCGTGGATTC | 57799 |
| rs35081719 | in-del | -/G | | | utr-variant-5-prime | RAB40C | GRCh38.p7 | 16:590281 | CGGCGCGGGGCGCAG[-/G]CGGCGCGGCCATGGG | 57799 |
| rs35238369 | snp | C/T | 0.439502 | 0.163061 | intron-variant | RAB40C | GRCh38.p7 | 16:599672 | AAGGTTTTGTTCCCT[C/T]GTGGCATCAGTCAGC | 57799 |
| rs35368117 | snp | A/G | 0.430136 | 0.173352 | intron-variant | RAB40C | GRCh38.p7 | 16:603051 | CGTGGCGCTGAAGCA[A/G]TCCTCCTGCCTCAGC | 57799 |
| rs35485339 | in-del | -/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:615548 | TTCTGGAAAGTTTCC[-/C]AGAGGGCCCAGAGCC | 57799 |
| rs35585285 | snp | G/T | 0.426354 | 0.177198 | intron-variant | RAB40C | GRCh38.p7 | 16:591445 | TTGGGACCCTGTCTC[G/T]AGCGTGCACAGATGA | 57799 |
| rs35588177 | in-del | -/A | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593932 | ATGCTTCATCCAGGA[-/A]GTGTGGGTGGTGCAC | 57799 |
| rs35609555 | in-del | -/G | | | utr-variant-3-prime, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629157 | GACTTTGAGGACCTG[-/G]ATGGTCCTGCATTCA | 57799 |
| rs35632779 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:592593 | GTAACTCCTGACTCA[A/G]GTGGTGGGCGGCCAA | 57799 |
| rs35642938 | snp | C/T | 0.496034 | 0.0443518 | intron-variant | RAB40C | GRCh38.p7 | 16:592249 | CTATTTGCTGAATTG[C/T]CTGCCTTTGGCTGCT | 57799 |
| rs35741114 | in-del | -/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:613180 | GAATCAAGAGCAGGG[-/G]ACAGCCGCCCTCACC | 57799 |
| rs35770441 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:614188 | ACTGCCGAACTCTAC[C/T]GCATCCCTATGGTGA | 57799 |
| rs35784676 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629400 | CCCTGCGCTGACCGG[A/G]CTGACCTGCCGCGGT | 57799 |
| rs35851877 | in-del | -/GT | | | intron-variant | RAB40C | GRCh38.p7 | 16:618911 | TGTGCTCAGGTGTGT[-/GT]ACTTGGAGCTGTGTG | 57799 |
| rs35915772 | snp | A/G | 0.460027 | 0.135605 | splice-donor-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629274 | AGCTGTGGTCCCCAC[A/G]TTTTGCTGTGTCTGG | 57799 |
| rs35940011 | in-del | -/G/GTG | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:618910 | GTGTGCTCAGGTGTG[-/G/GTG]TACTTGGAGCTGTGT | 57799 |
| rs36047476 | in-del | -/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:624280 | CTCTCCACCTCCCCC[-/C]AGCAGCAAATGAGCC | 57799 |
| rs36060490 | in-del | -/TCT | | | intron-variant | RAB40C | GRCh38.p7 | 16:604494 | ATACACGTGAGTCCT[-/TCT]GAGGGTGTTTCTCTA | 57799 |
| rs36085126 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596905 | GGATGGCGGCGCACT[C/T]TGATACAGGCAGTGC | 57799 |
| rs36155837 | snp | A/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:612408 | GCCCTGGCCTGTAGA[A/T]TCAAGAGCACGGGAC | 57799 |
| rs36175947 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:612362 | GCAGGGACAGCCGCC[C/T]TCGCCTGTAGAATCA | 57799 |
| rs36191177 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:612364 | AGGGACAGCCGCCTT[C/G]GCCTGTAGAATCAAG | 57799 |
| rs45593333 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:622503 | TCCCCTAGAGCACTC[A/G]CTCGTTCTTTTGTTT | 57799 |
| rs55634863 | snp | C/G | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:611815 | AGGGACAGCCGCCTT[C/G]GCCTGTAGAATCAAG | 57799 |
| rs55645201 | snp | A/G | 0.251014 | 0.249998 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593064 | CACTTCCAGGTCCCC[A/G]CAGGAGTCCTGTGGC | 57799 |
| rs55703450 | snp | C/T | 0.227959 | 0.249026 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593098 | GAGCAGAGAAGGAAG[C/T]GCCTCTGGGCTGTGG | 57799 |
| rs55715744 | snp | C/G | 0.229429 | 0.249152 | intron-variant | RAB40C | GRCh38.p7 | 16:616482 | TAGCTGGGATTAAAG[C/G]TGCCCACCACCACAC | 57799 |
| rs55730001 | snp | C/T | 0.153 | 0.230415 | intron-variant | RAB40C | GRCh38.p7 | 16:616528 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACTGTGT | 57799 |
| rs55732218 | snp | C/T | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:611813 | CAAGGGACAGCCGCC[C/T]TCGCCTGTAGAATCA | 57799 |
| rs55748561 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:618594 | GTGCACTCAGGGCCA[C/T]GTGTGTGTGCAGCCA | 57799 |
| rs55751178 | snp | A/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:599668 | CAGCAAGGTTTTGTT[A/C]CCTTGTGGCATCAGT | 57799 |
| rs55752159 | snp | A/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:599626 | CAGCAAGGTTTTGTT[A/C]CCTCGTGGCATTAAT | 57799 |
| rs55784745 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:599724 | CCCTCGTGGCATCAG[C/T]CAGCGTGGATTCGCA | 57799 |
| rs55798945 | snp | G/T | 0.362941 | 0.223034 | intron-variant | RAB40C | GRCh38.p7 | 16:619708 | GGTCTGGATCCTTCT[G/T]GGGGGAAGGTTCAGG | 57799 |
| rs55810041 | snp | A/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:606990 | GTGGCAGGCCGGCCC[A/T]GACAGACAGACTACC | 57799 |
| rs55845423 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:599740 | CAGCGTGGATTCGCA[A/G]GGTTTTGTTCCCTCG | 57799 |
| rs55846655 | snp | A/T | 0.259397 | 0.249823 | intron-variant | RAB40C | GRCh38.p7 | 16:592910 | CTCTGACATGCTCAC[A/T]GAAGTGGGGCCAGTA | 57799 |
| rs55913368 | snp | A/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:599654 | AATCAGCGTGGATTC[A/T]GCAAGGTTTTGTTCC | 57799 |
| rs55915938 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:611837 | AGAATCAAGAGCAGG[A/G]ACAGCCGCCCTGGCC | 57799 |
| rs55944622 | snp | A/C | 0.0391387 | 0.134304 | intron-variant | RAB40C | GRCh38.p7 | 16:599584 | CAGCAAGGTTTTGTT[A/C]CCTCGTGGCATCAGT | 57799 |
| rs56053470 | snp | G/T | 0.039522 | 0.134904 | intron-variant | RAB40C | GRCh38.p7 | 16:618930 | TGGAGCTGTGTGTGT[G/T]CACAGGTGTAGTGGG | 57799 |
| rs56088882 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:600023 | CAGTCAGCGTGGATT[C/T]GCAAGGTTTTGTTCC | 57799 |
| rs56096610 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:612422 | AATCAAGAGCAAGGG[A/G]CAGCCGCCTTCGCCT | 57799 |
| rs56175015 | snp | A/G | | | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628471 | CAGCCTCCTGTTCTC[A/G]GCAGCTTCTGTCGCT | 57799 |
| rs56197831 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:618625 | TGTGCACAGGTCTGG[C/T]GGGGGCACTGGGGCC | 57799 |
| rs56247649 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:601609 | TTCAGACAGGAGATT[C/T]TCATGAAAAATAGAA | 57799 |
| rs56260300 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:599719 | TTGTTCCCTCGTGGC[A/G]TCAGTCAGCGTGGAT | 57799 |
| rs56268356 | snp | A/G | 0.254105 | 0.249966 | intron-variant | RAB40C | GRCh38.p7 | 16:598575 | ACAAAAAAAAAAAAA[A/G]AAAAAGAAAAAAGAA | 57799 |
| rs56278520 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | RAB40C | GRCh38.p7 | 16:599320 | AGGCTGATGCCTGCC[C/T]GTGTCGGCCGGCCAC | 57799 |
| rs56311902 | snp | A/T | | | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595062 | GACCTCAAGTGATCC[A/T]CCTGCCTCGGGGGTT | 57799 |
| rs56791192 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | RAB40C | GRCh38.p7 | 16:619074 | GTAGTGGGTGCACTC[A/G]GCCATGTGTGTGTGC | 57799 |
| rs56867820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:600028 | AGCGTGGATTCGCAA[A/G]GTTTTGTTCCCTCGT | 57799 |
| rs56980831 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | RAB40C | GRCh38.p7 | 16:621906 | TGCTGCTGGCTTGTC[A/G]GCACACAGGTGGGCG | 57799 |
| rs57083715 | in-del | -/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:599653 | TAATCAGCGTGGATT[-/C]AGCAAGGTTTTGTTC | 57799 |
| rs57146999 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:626922 | CAGCCTGGCGACAGA[A/G]CGAGACCCGTCTCAA | 57799 |
| rs57189673 | snp | C/G | 0.264632 | 0.249571 | intron-variant | RAB40C | GRCh38.p7 | 16:616151 | AGTTCAGCTACTCAG[C/G]AGGCTGAGGCTAGAT | 57799 |
| rs57235517 | in-del | -/TATT/TATTTATTTATT | | | intron-variant | RAB40C | GRCh38.p7 | 16:616367 | ATTTATTTATTTATT[-/TATT/TATTTATTTATT]GAGTACTGTCACCCA | 57799 |
| rs57362118 | snp | A/T | 0.0256215 | 0.110247 | intron-variant | RAB40C | GRCh38.p7 | 16:627000 | CGCGCGCTCCCCCGC[A/T]CTAGGGGATGAGTCA | 57799 |
| rs57539332 | in-del | -/A | | | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:597938 | GACCCCATCTCTACA[-/A]AAAAAAAAAAAAAAA | 57799 |
| rs58060434 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | RAB40C | GRCh38.p7 | 16:609873 | GCTGTGTGCCTGGAG[C/G]GGGGAGCTGAGGCAC | 57799 |
| rs58170225 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:599640 | TACCTCGTGGCATTA[A/G]TCAGCGTGGATTCAG | 57799 |
| rs58178136 | snp | G/T | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:618902 | GTGTGCAGTGTGTGC[G/T]CAGGTGTGTACTTGG | 57799 |
| rs58206431 | in-del | -/AT | | | intron-variant | RAB40C | GRCh38.p7 | 16:618723 | CTCAGGGCCATGTGT[-/AT]GTGCAGGCATGTGCA | 57799 |
| rs58695020 | snp | C/T | 0.0333695 | 0.124785 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628879 | ACCCAGGACCCCCCG[C/T]GGTGGACTCCGCGGC | 57799 |
| rs58701150 | in-del | -/A | | | intron-variant | RAB40C | GRCh38.p7 | 16:620400 | CCATCTCAAAAAAAA[-/A]GGAGGAGCTGTGTGG | 57799 |
| rs58706644 | in-del | -/C | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:611904 | GTAGAATCAAGAGCA[-/C]GGGACAGCCGCCCTG | 57799 |
| rs58972886 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:618752 | CACAGGTCTGGCGGA[C/G]GCACTGGGGCCATGT | 57799 |
| rs59198063 | snp | A/C/G | 0.0387855 | 0.133914 | intron-variant | RAB40C | GRCh38.p7 | 16:599598 | TCCCTCGTGGCATCA[A/C/G]TCAGCGTGGATTCAG | 57799 |
| rs59401483 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | RAB40C | GRCh38.p7 | 16:622244 | AAAAAAGGTGTAAAC[A/G]TGCTCAGATGCATAT | 57799 |
| rs59677563 | in-del | -/AG | | | intron-variant | RAB40C | GRCh38.p7 | 16:618712 | GTAGTGGGTGCACTC[-/AG]GGCCATGTGTGTGCA | 57799 |
| rs60094426 | in-del | -/A | 0 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:601845 | AAAAAAAAAAAAAAA[-/A]GGCCGGATGCGGTGG | 57799 |
| rs60648394 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:599630 | AAGGTTTTGTTACCT[C/T]GTGGCATTAATCAGC | 57799 |
| rs60691303 | in-del | -/A | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:611800 | GTAGAATCAAGAGCA[-/A]GGGACAGCCGCCTTC | 57799 |
| rs60750561 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | RAB40C | GRCh38.p7 | 16:625712 | CAAGACCAGGAGCTA[C/T]GGGGCCACCCGGAAG | 57799 |
| rs60781812 | snp | G/T | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:618975 | TGTGTGTGCAGGCAT[G/T]TGCACAGGTCTGGCG | 57799 |
| rs60957680 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:618751 | GCACAGGTCTGGCGG[A/G]CGCACTGGGGCCATG | 57799 |
| rs61095721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594209 | GGGTGTGTGTGCCCG[A/G]GTCCTGGAAGACTTC | 57799 |
| rs61177993 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:600041 | AAGGTTTTGTTCCCT[C/T]GTGGCATCAGTCAGC | 57799 |
| rs61753371 | snp | C/T | 0.0438935 | 0.141492 | intron-variant | RAB40C | GRCh38.p7 | 16:590440 | ACAGTAACGGTAAGG[C/T]CCGGCCCGCGGCGCG | 57799 |
| rs61758748 | snp | A/G/T | 4.01744e-05 | 0.00448169 | synonymous-codon | RAB40C | GRCh38.p7 | 16:590417 | CGCGGCAGAGTCCCC[A/G/T]TACGCCTACAGTAAC | 57799 |
| rs62030900 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587367 | GGCACCCCTCTGTCC[A/G]TCCCTCCCTTCACTG | 57799 |
| rs62030901 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587823 | TTTTTTTTTTTTTTC[C/T]TGAGACAAGAGTCTC | 57799 |
| rs62030902 | snp | C/G | 0.496279 | 0.0429702 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588264 | ACTTCACAGCCAGGG[C/G]TCAAGTCTGGGCACA | 57799 |
| rs62030903 | snp | A/T | 0.496416 | 0.0421803 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588323 | TGACCCGCCAGGTTG[A/T]TTCCGGGTTAATGCC | 57799 |
| rs62030907 | snp | A/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:604236 | AGAGCTAGTTCTTTT[A/T]AATTTTTTTTTTTAA | 57799 |
| rs62030908 | snp | C/T | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:604517 | TGTTTCTCTAGAATA[C/T]ACGTGAGTCTTTCTG | 57799 |
| rs62030909 | snp | C/T | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:604519 | TTTCTCTAGAATACA[C/T]GTGAGTCTTTCTGAA | 57799 |
| rs62030910 | snp | C/T | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:604527 | GAATACACGTGAGTC[C/T]TTCTGAAGGTGTTTC | 57799 |
| rs62030911 | snp | C/T | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:604562 | GAATATATGTGAGTC[C/T]TTCTGAAGGTGTTTC | 57799 |
| rs62030912 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RAB40C | GRCh38.p7 | 16:604604 | CGTGAGTCCTTCTGA[A/G]GGTGTTTCTCTAGAA | 57799 |
| rs62030915 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:619084 | CACTCGGCCATGTGT[A/G]TGTGCAGGCATGTGC | 57799 |
| rs62030916 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:620322 | CGCTTGAACCCAGGA[A/G]GTGGAGGTTGCAGTG | 57799 |
| rs62030917 | snp | A/G | 0.458775 | 0.137524 | intron-variant | RAB40C | GRCh38.p7 | 16:622040 | CGCTGGCTGTACCTT[A/G]GGAGCTTCAGCCACA | 57799 |
| rs62623587 | snp | A/C | 0.202878 | 0.245519 | intron-variant | RAB40C | GRCh38.p7 | 16:625067 | TCCCGGGGGGATTCA[A/C]TGATGGACTGGCCGA | 57799 |
| rs63071260 | snp | A/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:604239 | GCTAGTTCTTTTAAA[A/T]TTTTTTTTTTAATTA | 57799 |
| rs63200160 | snp | C/T | 0.0205511 | 0.0992634 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587821 | TTTTTTTTTTTTTTT[C/T]CCTGAGACAAGAGTC | 57799 |
| rs66495935 | snp | A/C | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:612077 | GTAGCATCAAGAGCA[A/C]GGGACAGCCGCCCTG | 57799 |
| rs66495936 | in-del | -/A | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:612077 | GTAGAATCAAGAGCA[-/A]GGGACAGCCGCCCTG | 57799 |
| rs67275926 | in-del | -/T | | | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587804 | TTATTTTTGAGGCAC[-/T]TTTTTTTTTTTTTTT | 57799 |
| rs67519670 | in-del | -/A | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:612417 | GTAGAATCAAGAGCA[-/A]GGGACAGCCGCCCTG | 57799 |
| rs67746033 | in-del | -/GTG | | | intron-variant | RAB40C | GRCh38.p7 | 16:618908 | GTGTGTGCTCAGGTG[-/GTG]TGTACTTGGAGCTGT | 57799 |
| rs71139792 | in-del | -/TCCACGCTGACTGATGCCACGAGGGAACAAAACCTTGCGAATCCACGCTGACTGATGCCACGAGGTAACAAAACCTTGCGAA | 0 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:599692 | ACAAAACCTTGCGAA[lengthTooLong]TCCACGCTGACTGAT | 57799 |
| rs71139793 | in-del | -/A | 0.424659 | 0.17887 | intron-variant | RAB40C | GRCh38.p7 | 16:602248 | AAAAAAAACAAAACC[-/A]AAAAAAAAAAAAACA | 57799 |
| rs71299921 | in-del | -/A | 0.426813 | 0.17674 | intron-variant | RAB40C | GRCh38.p7 | 16:604061 | CAGAACGAGAGTCTC[-/A]AAAAAAAAAAAAAAG | 57799 |
| rs71299922 | in-del | -/GGGCAGCAGGCCCAGTGAAGGGAGGGACGGACTCTG | 0.5 | 0 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587466 | ACCCAGATGGGTCTA[lengthTooLong]GGGCAGCAGGCCCAG | 57799 |
| rs71378522 | snp | C/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593555 | TCCTTCAGCTCACAC[C/G]GGATCGCTTACCTGC | 57799 |
| rs71378523 | snp | C/T | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:612023 | AGGGACAGCCGCCTT[C/T]GCCTGTAGAATCAAG | 57799 |
| rs71378524 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | RAB40C | GRCh38.p7 | 16:612066 | CGCCCTGGCCTGTAG[A/C]ATCAAGAGCAAGGGA | 57799 |
| rs71378525 | snp | A/C | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:613232 | CGCCCTGGCCTGTAG[A/C]ATCAAGAGCAGGGAC | 57799 |
| rs71378526 | snp | A/C | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:613266 | CGCCCTGGCCTGTAG[A/C]ATCAAGAGCAGGGAC | 57799 |
| rs71378527 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:613285 | AAGAGCAGGGACAGC[C/T]GCCCTTGCTTGTAGA | 57799 |
| rs71388247 | multinucleotide-polymorphism | CAG/GAA | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:613122 | CTTGATTCTACAGGC[CAG/GAA]GGCGGCTGTCCCTTG | 57799 |
| rs71388248 | in-del | GCTCTTGAAT/TGCTCTTGATG | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:611858 | AGGGCGGCTGTCCCT[GCTCTTGAAT/TGCTCTTGATG]CTACAGGCCAGGGCG | 57799 |
| rs71388250 | multinucleotide-polymorphism | CAG/GAA | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:612158 | CTTGATTCTACAGGC[CAG/GAA]GGCGGCTGTCCCTGC | 57799 |
| rs71388252 | multinucleotide-polymorphism | CAG/GAA | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:611813 | CTTGATTCTACAGGC[CAG/GAA]GGCGGCTGTCCCTTG | 57799 |
| rs71391137 | in-del | -/GCCCCCA | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:603789 | AGCCCCCAGCCCCCA[-/GCCCCCA]GCAGTCGGCTTCCAT | 57799 |
| rs71391139 | in-del | -/C | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:612936 | GTAGAATCAAGAGCA[-/C]GGGACAGCCGCCCTG | 57799 |
| rs71391141 | in-del | -/C | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:613177 | GTAGAATCAAGAGCA[-/C]GGGACAGCCGCCCTC | 57799 |
| rs71391142 | multinucleotide-polymorphism | CA/GG | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:613192 | AGGGACAGCCGCCCT[CA/GG]CCTGTAGAATCAGCA | 57799 |
| rs71391143 | in-del | CC/T | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:626343 | GCTGATGACCCCCCC[CC/T]CAGGGTGCCGCCGTG | 57799 |
| rs71843151 | in-del | -/GTC | | | intron-variant | RAB40C | GRCh38.p7 | 16:622408 | CGGCACCGTGGACAC[-/GTC]TGTAGACGCTGAGGA | 57799 |
| rs72186889 | in-del | -/CA | 0.0360663 | 0.129354 | intron-variant | RAB40C | GRCh38.p7 | 16:591218 | CATGGTCTGGGATCT[-/CA]GGGGAAGGTGTCATG | 57799 |
| rs72767868 | snp | A/G | 0.243633 | 0.249919 | intron-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596246 | ATCGGGGAGCTGAGA[A/G]GTGGGCGGGAAGGAC | 57799 |
| rs72767874 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RAB40C | GRCh38.p7 | 16:605292 | CAATGCATGAGAGTT[C/T]CAGGTGCTCCACATC | 57799 |
| rs72767876 | snp | A/G | 0.0744748 | 0.178019 | intron-variant | RAB40C | GRCh38.p7 | 16:605809 | TTGGGACGTACTGAG[A/G]AGTGGAAGCTGGGCT | 57799 |
| rs72767879 | snp | C/G | 0.261608 | 0.24973 | intron-variant | RAB40C | GRCh38.p7 | 16:607073 | GAGGGTGCTACGCAG[C/G]CTCAGCAGCCAGCCT | 57799 |
| rs72767885 | snp | G/T | 0.251859 | 0.249993 | intron-variant | RAB40C | GRCh38.p7 | 16:619857 | CACTGAAGTGTAGTC[G/T]GTGTTGGATCTGATG | 57799 |
| rs72767889 | snp | C/T | 0.167484 | 0.23599 | intron-variant | RAB40C | GRCh38.p7 | 16:624601 | GGACAGTGCCCTCTT[C/T]TTTCAGCCTCAGCCT | 57799 |
| rs73483590 | snp | A/G | 0.0858192 | 0.188533 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588023 | GATGTTGGCCAAGCT[A/G]GTCCTGACCTCAGGT | 57799 |
| rs73483598 | snp | A/G | 0.0955749 | 0.196603 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593151 | TCTCAAGGTTAAGAC[A/G]TGCACAGCACAAGGA | 57799 |
| rs73485414 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RAB40C | GRCh38.p7 | 16:604269 | ATTTTTCTTGTAAAA[C/T]ACAGAAAACACGTCA | 57799 |
| rs73485415 | snp | A/G | 0.100231 | 0.200173 | intron-variant | RAB40C | GRCh38.p7 | 16:605430 | GCGGACAGGCATGCC[A/G]GCCTGAGAAAGCATC | 57799 |
| rs73485420 | snp | A/G | 0.0966517 | 0.197444 | intron-variant | RAB40C | GRCh38.p7 | 16:615625 | CTTTCAGTTTCTCTT[A/G]GACTGACCTTTTCCT | 57799 |
| rs73485427 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RAB40C | GRCh38.p7 | 16:617345 | GAACCCTTAGAGAAA[C/T]AGGAAGGCGTCCTGT | 57799 |
| rs73485428 | snp | A/G | 0.084364 | 0.187256 | intron-variant | RAB40C | GRCh38.p7 | 16:617554 | TTCACCTTAAAAAGC[A/G]TTTCCCAGCGGGGTG | 57799 |
| rs73485431 | snp | A/G/T | 0.0252325 | 0.109451 | intron-variant | RAB40C | GRCh38.p7 | 16:619480 | ACTGGATCTGCTGGC[A/G/T]AATGTGAGGCCGGAA | 57799 |
| rs73485436 | snp | A/C | 0.0402882 | 0.136092 | intron-variant | RAB40C | GRCh38.p7 | 16:619784 | GAAGCTGCCCAGGTG[A/C]GAGGGGGATGGACAC | 57799 |
| rs73485439 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | RAB40C | GRCh38.p7 | 16:619995 | GGGCCTGCAGGCTCC[A/G]TGCCATCCCTGTGAG | 57799 |
| rs73485447 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | RAB40C | GRCh38.p7 | 16:622972 | TTGGTTTCTCACTCC[A/G]TGGTCATTTGGGTCC | 57799 |
| rs73485459 | snp | C/T | 0.00580474 | 0.05356 | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629563 | GCAGATGGCCTGGGG[C/T]GGACTGTCCCCAACA | 57799 |
| rs74000829 | snp | A/G | 0.0399052 | 0.1355 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587668 | GGATGACCCTTTCTT[A/G]TCCCAGGAGGTGGGA | 57799 |
| rs74000830 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588885 | ACTTCACCGAGAGAG[A/G]CAGGACCATCCCCAC | 57799 |
| rs74000831 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | RAB40C | GRCh38.p7 | 16:591098 | AGGGAAGCTGTCATG[A/G]GTCTGGGATCATCTG | 57799 |
| rs74000834 | snp | A/C/G | 0.0356815 | 0.128715 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596547 | GCAGGGAAAGGTGTC[A/C/G]GCGTCCAGCATCCTG | 57799 |
| rs74000835 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | RAB40C | GRCh38.p7 | 16:598856 | CCTCATGTCAACCCT[A/G]AGTGAAGGTGTAGGC | 57799 |
| rs74000836 | snp | C/T | 0.100588 | 0.200439 | intron-variant | RAB40C | GRCh38.p7 | 16:599588 | AAGGTTTTGTTCCCT[C/T]GTGGCATCAGTCAGC | 57799 |
| rs74000837 | snp | C/T | 0.350982 | 0.228698 | intron-variant | RAB40C | GRCh38.p7 | 16:599695 | CAGTCAGCGTGGATT[C/T]GCAAGGTTTTGTTCC | 57799 |
| rs74000866 | snp | A/G | 0.0655868 | 0.168795 | intron-variant | RAB40C | GRCh38.p7 | 16:605652 | CTCCTTCCCCGCGCC[A/G]AGTGGTCTCCCGTGT | 57799 |
| rs74000869 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | RAB40C | GRCh38.p7 | 16:610303 | GGTTGTGTTCAGGTC[A/G]GCTGAGAGGCAGCGC | 57799 |
| rs74000871 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | RAB40C | GRCh38.p7 | 16:611137 | GAGCATCCCAGAGCA[A/G]CCTCTGATTCAAGAG | 57799 |
| rs74000876 | snp | C/T | 0.00279043 | 0.0372482 | intron-variant | RAB40C | GRCh38.p7 | 16:625101 | GACACTTAGCTTCCA[C/T]AGCTGCACGTCCCCC | 57799 |
| rs74000878 | snp | A/G | 0.089084 | 0.191327 | intron-variant | RAB40C | GRCh38.p7 | 16:626492 | GCAGCTTTGTGTTGT[A/G]TCATCTGCTCTTCCT | 57799 |
| rs74361711 | snp | C/G | 0.0178098 | 0.0926698 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588008 | AGAGGGGGTTATCAC[C/G]ATGTTGGCCAAGCTG | 57799 |
| rs74423338 | snp | A/G | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:608335 | CTGGCCCCGCCCTCA[A/G]CCTGTGGGGATTAGT | 57799 |
| rs74473099 | snp | C/T | 0.5 | 0 | intron-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595605 | TAACTTTTTTCTTCT[C/T]TTTTTTTTTTTTTTT | 57799 |
| rs74610889 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RAB40C | GRCh38.p7 | 16:600069 | AGCGTGGATTTGCAA[A/G]GTTTTGTTCCCTTGT | 57799 |
| rs74777284 | snp | A/G | 0.0356179 | 0.128609 | intron-variant | RAB40C | GRCh38.p7 | 16:617311 | CCTGGGTGAGGACAC[A/G]AATGCCGAAGGGAGA | 57799 |
| rs74842306 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | RAB40C | GRCh38.p7 | 16:626239 | AGGTCCCTTGGCAAC[A/G]CGCAGTAGGGGCTCG | 57799 |
| rs74848726 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593236 | ATCAGGGTGAAGTTG[A/G]TGGATCTGAGGGTTT | 57799 |
| rs74953164 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | RAB40C | GRCh38.p7 | 16:605417 | CAATACAGTGAGTGC[A/G]GACAGGCATGCCGGC | 57799 |
| rs74971514 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | RAB40C | GRCh38.p7 | 16:611395 | AGCAGCTATGGCCTT[C/T]GTGGCAATCGTGGTG | 57799 |
| rs75020777 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | RAB40C | GRCh38.p7 | 16:620522 | TTAAAAAATATGGGG[C/T]GCAGTTATGTTGGAT | 57799 |
| rs75168193 | snp | A/G | 0.444444 | 0.157135 | intron-variant | RAB40C | GRCh38.p7 | 16:614618 | ACTCTACCACATCCC[A/G]ATGGTGAACTGCTAA | 57799 |
| rs75238938 | snp | A/G | 0.030278 | 0.119257 | intron-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596257 | GAGAGGTGGGCGGGA[A/G]GGACACAAGGGAGGG | 57799 |
| rs75323697 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | RAB40C | GRCh38.p7 | 16:624571 | AAGAGGCTCTAAAAA[C/T]CCTAATTTTCAGATG | 57799 |
| rs75394749 | snp | G/T | 0.0513262 | 0.151752 | intron-variant | RAB40C | GRCh38.p7 | 16:620964 | CAGTTCATAAGCTCT[G/T]CATTTGCCAGGCTGA | 57799 |
| rs75405768 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | RAB40C | GRCh38.p7 | 16:621211 | CGGGCCTCTGACCGC[C/T]GTGACTGAGCATTTG | 57799 |
| rs75445413 | snp | A/C | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:625216 | ACACCATGGAAGGCG[A/C]CCACCCCCCTGCTGC | 57799 |
| rs75446372 | snp | C/T | 0.00360985 | 0.0423307 | synonymous-codon | RAB40C | GRCh38.p7 | 16:590346 | CTGCTCAAGTTCCTG[C/T]TGGTGGGCGACAGCG | 57799 |
| rs75455987 | snp | A/G | 0 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:614281 | CTGCCTAACTCTACC[A/G]CATCCCGATGGTGAA | 57799 |
| rs75588265 | snp | A/T | 0 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:612788 | GCCCTGGCCTGTAGA[A/T]TCAAGAGCAGGGACA | 57799 |
| rs75593711 | in-del | -/CCCCAGC | | | intron-variant | RAB40C | GRCh38.p7 | 16:603791 | CCCCCAGCCCCCAGC[-/CCCCAGC]AGTCGGCTTCCATCA | 57799 |
| rs75839021 | snp | C/T | 0 | 0 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587807 | TTTTTGAGGCACTTT[C/T]TTTTTTTTTTTTTTC | 57799 |
| rs75949776 | snp | C/G | 0.5 | 0 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588863 | GCTCACCCGTTCCGA[C/G]TGAGTAACTTCACCG | 57799 |
| rs75961884 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RAB40C | GRCh38.p7 | 16:603200 | TGTGGGTTTTAAGGC[A/G]TTAAGTAAAAGCTCT | 57799 |
| rs76284418 | snp | A/G | 0 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:614308 | TGAACTGCTAACTCT[A/G]CCACATCCCGATGGT | 57799 |
| rs76469414 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:624770 | GCCTGTGATGTCACC[A/G]TTTCGCCCGACAGGG | 57799 |
| rs76494279 | snp | A/G | 0.0117317 | 0.075685 | missense | RAB40C | GRCh38.p7 | 16:590403 | AGCCTGCAGGACGGC[A/G]CGGCAGAGTCCCCGT | 57799 |
| rs76581531 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | RAB40C | GRCh38.p7 | 16:613880 | CCCTGGACTTGAGGA[A/G]CAGGATTCCTGACTG | 57799 |
| rs76611479 | snp | G/T | 0.444444 | 0.157135 | intron-variant | RAB40C | GRCh38.p7 | 16:599788 | GATTCGCAAGGTTTT[G/T]TTCCCTCGTGGCATC | 57799 |
| rs76673239 | snp | C/T | 0 | 0 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:597475 | AGCCATCTAGCATCT[C/T]TTTTTTTTTTTTAAT | 57799 |
| rs76675507 | snp | A/G | 0.375 | 0.216506 | intron-variant | RAB40C | GRCh38.p7 | 16:614401 | AACTGCCTAAACCTC[A/G]TCCCGATGGTGAACT | 57799 |
| rs76745387 | snp | A/T | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:591566 | GAGTTACTGAACATT[A/T]GTTTTGTTTTGTTTT | 57799 |
| rs76926092 | snp | C/G | 0.0360663 | 0.129354 | intron-variant | RAB40C | GRCh38.p7 | 16:608201 | CAGGGCAGCTCCAGA[C/G]AGAATGAGTGCTGAG | 57799 |
| rs76954615 | snp | C/T | 0.444444 | 0.157135 | intron-variant | RAB40C | GRCh38.p7 | 16:600082 | AAAGTTTTGTTCCCT[C/T]GTGGCATCATACTCC | 57799 |
| rs77241726 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594821 | TTGCTCGTCTTCCTT[C/T]TTTTTTTTTTTTTTT | 57799 |
| rs77548523 | in-del | -/TG | | | intron-variant | RAB40C | GRCh38.p7 | 16:604521 | TCTCTAGAATACACG[-/TG]AGTCTTTCTGAAGGT | 57799 |
| rs77599282 | snp | A/C | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:622228 | TAGGTCGAGTTGATC[A/C]AAAAAAGGTGTAAAC | 57799 |
| rs77835338 | snp | C/T | 0.0596104 | 0.162024 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593027 | CTTAGAAAGACACCA[C/T]GTGCTCTCAGGGCCC | 57799 |
| rs78183845 | snp | A/C | 0.0356815 | 0.128715 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:597519 | GACAGAGTCTTGCTC[A/C]GTTACCCAGGGTGTA | 57799 |
| rs78273064 | snp | C/G | 0.0360663 | 0.129354 | intron-variant | RAB40C | GRCh38.p7 | 16:609057 | GAGTTGGAGGCTGCA[C/G]TGAGCCTTGGCCTCA | 57799 |
| rs78273069 | snp | A/G | 0.375 | 0.216506 | intron-variant | RAB40C | GRCh38.p7 | 16:614468 | ACTCTACCACATCCC[A/G]ATGGTGAACTGCTAA | 57799 |
| rs78736508 | snp | A/G | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:614189 | CTGCCGAACTCTACC[A/G]CATCCCTATGGTGAA | 57799 |
| rs78929374 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:604870 | TTTGAGACCAGCCTG[A/G]CCAACATGGTGAAAC | 57799 |
| rs78957529 | snp | A/T | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:591560 | TGTAATGAGTTACTG[A/T]ACATTTGTTTTGTTT | 57799 |
| rs78996934 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | RAB40C | GRCh38.p7 | 16:621987 | GTTGCTCCTGGGCAG[A/G]GCCTGGGTGCAGGGA | 57799 |
| rs79030179 | snp | A/C/T | 0.0449073 | 0.143139 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628907 | GGCACATGCTTCCCA[A/C/T]GGTGGTCCCACGGAG | 57799 |
| rs79049529 | snp | C/G | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:602806 | AACTCCTGGGCTCAA[C/G]TGATTCTCTCACCTT | 57799 |
| rs79106972 | snp | A/G | 0 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:614551 | AACTGCCTAAACCTC[A/G]TCCCGATGGTGAACT | 57799 |
| rs79161193 | snp | G/T | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:604075 | TCTTTTTTTTTTTTT[G/T]GAGACTCTCGTTCTG | 57799 |
| rs79231406 | snp | A/C | 0.444444 | 0.157135 | intron-variant | RAB40C | GRCh38.p7 | 16:620292 | CAGCTACTTAGGAGG[A/C]TGAGGCAGGAGAATC | 57799 |
| rs79234649 | in-del | -/CCT | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594817 | GGTTTTGCTCGTCTT[-/CCT]TTTTTTTTTTTTTTT | 57799 |
| rs79319806 | snp | A/C | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:617591 | CTCACGCCTGTCATC[A/C]CAGCACTTTGGGAGG | 57799 |
| rs79327619 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:598640 | CCAATTACTTGGGAG[C/G]CTGAGGTGGGAAACT | 57799 |
| rs79366855 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | RAB40C | GRCh38.p7 | 16:605184 | GAGCCGTGATTGTTC[C/T]GCTGCACTCCAGCCT | 57799 |
| rs79422067 | snp | A/C | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:598563 | AGACTCTGTCTCACA[A/C]AAAAAAAAAAAAAAA | 57799 |
| rs79575943 | snp | A/G | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:614186 | GAACTGCCGAACTCT[A/G]CCGCATCCCTATGGT | 57799 |
| rs79582746 | snp | C/T | 0.444444 | 0.157135 | intron-variant | RAB40C | GRCh38.p7 | 16:600064 | CAGTCAGCGTGGATT[C/T]GCAAAGTTTTGTTCC | 57799 |
| rs79590716 | snp | C/G/T | 0.0123036 | 0.0774623 | intron-variant | RAB40C | GRCh38.p7 | 16:600554 | TCAAGAGATCAAGAC[C/G/T]GTTCTGACCAACATG | 57799 |
| rs79597513 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594839 | TTTTTTTTTTTTTTT[A/T]GACGAAGTCTTACTC | 57799 |
| rs79629296 | snp | A/G | 0.375 | 0.216506 | intron-variant | RAB40C | GRCh38.p7 | 16:614341 | ACTGCTAACTCTGCC[A/G]CATCCCGATGGTGAA | 57799 |
| rs79650431 | snp | A/G | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:604499 | CGTGAGTCCTTCTGA[A/G]GGTGTTTCTCTAGAA | 57799 |
| rs79698616 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RAB40C | GRCh38.p7 | 16:606105 | GTTATTGCTGACACA[C/T]AGTCCTCTCGGTCCT | 57799 |
| rs79735412 | snp | A/T | 0 | 0 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587806 | ATTTTTGAGGCACTT[A/T]TTTTTTTTTTTTTTT | 57799 |
| rs79765771 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | RAB40C | GRCh38.p7 | 16:603925 | TCTTCTTTTTTTGTT[C/T]CCAAGTGGTATTCCT | 57799 |
| rs79780732 | snp | A/G | 0.00517822 | 0.0506191 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:589115 | CGCAGTGAGCACGTC[A/G]GGCCGGGTCTTGAGC | 57799 |
| rs79942353 | snp | A/C | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:591562 | TAATGAGTTACTGAA[A/C]ATTTGTTTTGTTTTG | 57799 |
| rs80010439 | snp | A/T | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:611963 | GCCCTGGCCTGTAGA[A/T]TCAAGAGCAAGGGAC | 57799 |
| rs80106001 | snp | A/G | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:612567 | GAGCACGGGACAGCC[A/G]CCCTGGCCTGTAGAA | 57799 |
| rs80201629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:604489 | CTAGAATACACGTGA[A/G]TCCTTCTGAGGGTGT | 57799 |
| rs80331613 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594840 | TTTTTTTTTTTTTTA[G/T]ACGAAGTCTTACTCT | 57799 |
| rs111247309 | snp | A/G | 0.261884 | 0.249717 | intron-variant | RAB40C | GRCh38.p7 | 16:607466 | TGATATTGCGCCACC[A/G]CACTCCGGCCTGGAC | 57799 |
| rs111254785 | snp | A/C | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:599873 | TCGCAAGGTTTTGTT[A/C]CCTCGTGGCATCAGT | 57799 |
| rs111283208 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:591621 | TTTTTGAGACGGAGT[C/G]TCACTCTGTCGCCAG | 57799 |
| rs111286429 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:611952 | TTGATTCTACAGGCC[A/G]GGGCGGCTGTCCCTG | 57799 |
| rs111308722 | snp | A/C | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:599955 | TCGCAAGGTTTTGTT[A/C]CCTCGTGGCATCAGT | 57799 |
| rs111366065 | snp | C/T | | | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588983 | GGCCCGCGGACGCAG[C/T]CGCCTCGCTCGCCCA | 57799 |
| rs111467675 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:627988 | AGCCTGGGTGTGGCC[C/T]GGTGGTGGTGCACTG | 57799 |
| rs111472301 | snp | A/C | 0.0356815 | 0.128715 | utr-variant-5-prime, upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:589417 | AGGCGGCACAGCCTG[A/C]GAGGGGCTTTCGTTT | 57799 |
| rs111482111 | snp | C/G | 0 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:618478 | CACTGCAGCCTCCCC[C/G]TCCCGGGTTCAAGCG | 57799 |
| rs111490416 | snp | C/T | 0.271702 | 0.249056 | intron-variant, upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:589819 | GCCGTGTGGGAAAGG[C/T]GGGGGAGGGGCGGTC | 57799 |
| rs111508882 | snp | G/T | 0 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:615035 | TTGTTCCTTCTTGTC[G/T]TGGAAACGAGGACCC | 57799 |
| rs111651971 | snp | C/T | 0 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:626156 | CCAGCCCTGAGGTCC[C/T]CGAACCTGGGCTGCC | 57799 |
| rs111742284 | snp | C/G | 0.251014 | 0.249998 | intron-variant | RAB40C | GRCh38.p7 | 16:622627 | ATTCTCCTGCCTCAG[C/G]CTCCCGAGTAGCTAG | 57799 |
| rs111826295 | snp | A/T | 0.213333 | 0.247296 | intron-variant | RAB40C | GRCh38.p7 | 16:617791 | GAAGTTGCAGTGAGC[A/T]GAGATTGCACCACTG | 57799 |
| rs111829588 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:607532 | CGGGGGGCCGGGCGC[A/G]GTGGCTCACGCCTGT | 57799 |
| rs111923530 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | RAB40C | GRCh38.p7 | 16:620122 | GAGTTGGGGCTGGTG[C/T]GGTGGTTCACGCCTG | 57799 |
| rs111927633 | snp | C/T | 0.0228947 | 0.104514 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587836 | TCCTGAGACAAGAGT[C/T]TCACTCTGTAGCCCA | 57799 |
| rs111956308 | snp | G/T | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:618658 | GTGTGCAGTGTGTGC[G/T]CAGGTGTGGTGTACT | 57799 |
| rs111972007 | snp | C/T | 0 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:617875 | AAGCATTTCCCAGAA[C/T]GTCAGCGTTGATGAG | 57799 |
| rs112064138 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | RAB40C | GRCh38.p7 | 16:621556 | AGGCCCTTCACGTGC[C/T]GCCGAAGGCCGGGCT | 57799 |
| rs112181304 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:619336 | CAGGGCCATGTGTGT[C/G]TGCAGCCATGTGCAC | 57799 |
| rs112185160 | snp | A/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:614575 | GTGAACTGCCTAACT[A/C]TACCGCATCCCGATG | 57799 |
| rs112203452 | snp | C/T | 0.0748431 | 0.178382 | intron-variant | RAB40C | GRCh38.p7 | 16:619283 | GCAGGTGTGGTGTAC[C/T]TGGAGCTGTGTGTGT | 57799 |
| rs112271354 | snp | G/T | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:614291 | CTACCACATCCCGAT[G/T]GTGAACTGCTAACTC | 57799 |
| rs112289264 | snp | A/C | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:599996 | TCGCAAGGTTTTGTT[A/C]CCTCGTGGCATCAGT | 57799 |
| rs112303169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:600940 | GGTGTGTGGCAGCTG[C/T]GTGAGGCTCTCCTGG | 57799 |
| rs112334434 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:618790 | GTGTGCAGGTGTGGT[A/G]TACTTGGAGCTGTGT | 57799 |
| rs112436266 | snp | A/C | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:599914 | TCGCAAGGTTTTGTT[A/C]CCTCGTGGCATCAGT | 57799 |
| rs112467994 | snp | A/G | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:623566 | GACTGAGGCAGGAGA[A/G]TGGCGTGAACCCGGA | 57799 |
| rs112536311 | snp | G/T | 0 | 0 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:597739 | AGCAATCCGCCCGCC[G/T]CAGCTTCCCAAAGTT | 57799 |
| rs112567902 | snp | G/T | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:619143 | GTGTGCAGTGTGTGC[G/T]CAGGTGTGGTGTACT | 57799 |
| rs112586174 | snp | A/G | 0.00795532 | 0.062565 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628443 | AGCGGTGCAGACCCC[A/G]GGCACCTGCGTGCAG | 57799 |
| rs112610137 | snp | C/G | 0.256619 | 0.249912 | intron-variant | RAB40C | GRCh38.p7 | 16:602045 | GCAAGAGAATCGCTT[C/G]AACCCAGGAGGCAGA | 57799 |
| rs112618169 | snp | C/G | 0.0460142 | 0.144533 | intron-variant | RAB40C | GRCh38.p7 | 16:605338 | TGTTGTCAGCTTTCC[C/G]TCTTTTAATTAATCA | 57799 |
| rs112713499 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:589798 | GGCGTCCGCTGTCTC[C/T]GCAACGCCGTGTGGG | 57799 |
| rs112736544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:606629 | GGTTGGCAGAATTCC[A/G]TTCTTGCTGGTGGTA | 57799 |
| rs112767802 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:599618 | CGTGGATTCAGCAAG[A/G]TTTTGTTACCTCGTG | 57799 |
| rs112803692 | snp | C/T | 0 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:614317 | AACTCTGCCACATCC[C/T]GATGGTGAACTGCTA | 57799 |
| rs112890089 | snp | A/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:607077 | GTGCTACGCAGGCTC[A/T]GCAGCCAGCCTCCCT | 57799 |
| rs112902525 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RAB40C | GRCh38.p7 | 16:615777 | GACCAGCTTAGCCAA[C/T]GTGGCAAAACCCCGT | 57799 |
| rs113086265 | snp | A/G | 0 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:610417 | AGGAGGAGAGCAGGG[A/G]GAAGGGTGGCAGGAG | 57799 |
| rs113097297 | snp | C/T | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:599736 | CAGTCAGCGTGGATT[C/T]GCAAGGTTTTGTTCC | 57799 |
| rs113240348 | snp | C/G | 0 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:610698 | CTCCAGGCCTCTCCT[C/G]GGTCACTGCTCTGTG | 57799 |
| rs113311435 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:627731 | TGTCCACACAGCTGC[C/T]TCAGAAGCGCCGGGC | 57799 |
| rs113333691 | snp | A/G | 0 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:590666 | CCCAGCGGGGACGGT[A/G]CCATGGACCCGGGGT | 57799 |
| rs113334650 | snp | A/T | 0.5 | 0 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587558 | ATCTCACCCTATGGA[A/T]AGGTTCCTGAACCCA | 57799 |
| rs113507772 | snp | A/G | 0 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:613499 | GCCTGGCTTCTGCAC[A/G]CCGGCTGGCACTTGC | 57799 |
| rs113565584 | snp | A/C | 0 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:599750 | TCGCAAGGTTTTGTT[A/C]CCTCGTGGCATCAGT | 57799 |
| rs113609809 | snp | C/T | 0.0603597 | 0.1629 | intron-variant | RAB40C | GRCh38.p7 | 16:623398 | CTCACGCCTGTCATC[C/T]CAGCACTTTGGGAGG | 57799 |
| rs113639315 | snp | A/G | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:606368 | GGTGTTGGCTGACAC[A/G]CAGTCCTCTCGGTCC | 57799 |
| rs113743432 | snp | A/G | | | missense | RAB40C | GRCh38.p7 | 16:617250 | TGCTGGACGGCCGGC[A/G]CGTGAAGCTGGAGCT | 57799 |
| rs113772211 | in-del | -/G | 0 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:622627 | ATTCTCCTGCCTCAG[-/G]CTCCCGAGTAGCTAG | 57799 |
| rs113843749 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RAB40C | GRCh38.p7 | 16:600122 | TGGTTTGGGACTCCC[A/G]TGGCCCCCTTGATGT | 57799 |
| rs113968358 | snp | C/T | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:592071 | GAATGGGATGTGGCC[C/T]CAGATGAACTGGGAG | 57799 |
| rs113983612 | in-del | -/T | 0 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:620836 | CCCAGCCACCCCCCC[-/T]CGACGGGCTCCACCG | 57799 |
| rs114022256 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | RAB40C | GRCh38.p7 | 16:599524 | TCGATAGGCATGTAC[A/G]TGAAAATGCACACCC | 57799 |
| rs114028085 | snp | C/G | 0.0685596 | 0.171987 | intron-variant | RAB40C | GRCh38.p7 | 16:617396 | CCACTTACACAGCCC[C/G]TGTTTAAACATAGAA | 57799 |
| rs114220093 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | RAB40C | GRCh38.p7 | 16:590524 | CCCGGCCCTTCCAAG[A/C]GCCGCCGAACGTTCC | 57799 |
| rs114359833 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | RAB40C | GRCh38.p7 | 16:619872 | GGTGTTGGATCTGAT[C/G]TCTTCTACCTGCTGG | 57799 |
| rs114425927 | snp | C/G | 0.0248432 | 0.108648 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628841 | GCACGACATGGCCAG[C/G]ACGCAGAAGGAGCCC | 57799 |
| rs114534041 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596521 | TGTCATCCGCCGGGC[A/G]TTTGGAGTAAGCAGG | 57799 |
| rs114537858 | snp | C/T | 0.00835141 | 0.0640778 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588574 | GCCGCTTAGTCAGGC[C/T]ATGTCTTCAGCTCTG | 57799 |
| rs114538166 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RAB40C | GRCh38.p7 | 16:591899 | TGCGCCTGGCCTGAA[C/T]GTTTGTTTTTAACTT | 57799 |
| rs114738208 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:623116 | CTCAGGGCAGCAGCC[A/G/T]GGAGGTGTGGCCAGG | 57799 |
| rs114995811 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | RAB40C | GRCh38.p7 | 16:613395 | GGGACTGCCGCCCTC[A/G]CCTGTAGAATCAAGA | 57799 |
| rs115029438 | snp | C/T | 0.0562307 | 0.157967 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:627770 | CACCTGAGCCGGGTG[C/T]GAGGAGGAGCATGCA | 57799 |
| rs115032082 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RAB40C | GRCh38.p7 | 16:591392 | CCGGGGAAGGTGTCA[C/T]GGACCCAGGTCTGGT | 57799 |
| rs115059486 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | RAB40C | GRCh38.p7 | 16:622971 | TTTGGTTTCTCACTC[C/T]GTGGTCATTTGGGTC | 57799 |
| rs115173162 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RAB40C | GRCh38.p7 | 16:590968 | GGGGTCCGGGGAAAG[A/G]TGTCATGGTCCCGGT | 57799 |
| rs115229224 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | RAB40C | GRCh38.p7 | 16:619416 | GGTGGGTGCGCTTGG[C/T]CACCCTCGTTTCTGT | 57799 |
| rs115379997 | snp | A/G | 0.0520825 | 0.152737 | intron-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595997 | TTGAATGTTAAGTTT[A/G]TCCAGAGGCCAGATG | 57799 |
| rs115498939 | snp | C/G/T | 0.0142736 | 0.0832652 | intron-variant | RAB40C | GRCh38.p7 | 16:607087 | GGCTCAGCAGCCAGC[C/G/T]TCCCTCGGCTGCCTT | 57799 |
| rs115517847 | snp | C/T | 0.0013978 | 0.0263997 | intron-variant | RAB40C | GRCh38.p7 | 16:625874 | CACCCTGCGTTTGTG[C/T]GTCTGCTGAGTTCTG | 57799 |
| rs115577242 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | RAB40C | GRCh38.p7 | 16:611104 | CAGGATGGGTGGGAC[A/G]CAGACGTCCAGCGGG | 57799 |
| rs115589519 | snp | A/C | 0.0225045 | 0.103662 | intron-variant | RAB40C | GRCh38.p7 | 16:620470 | TGCTTTTAAGTATTT[A/C]GTGATTTTTCTGCAA | 57799 |
| rs115606615 | snp | C/G | 0.0520825 | 0.152737 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:597752 | CCTCAGCTTCCCAAA[C/G]TTGGTGGAATTACAG | 57799 |
| rs115668489 | snp | A/C/G | 0.0142736 | 0.0832652 | intron-variant | RAB40C | GRCh38.p7 | 16:609874 | CTGTGTGCCTGGAGG[A/C/G]GGGAGCTGAGGCACG | 57799 |
| rs115762526 | snp | A/G | 0.0146672 | 0.084371 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593402 | GTGTTAACCTCCATT[A/G]CTTTCTCTCCTTTGT | 57799 |
| rs115810040 | snp | A/G | 0.0596104 | 0.162024 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628304 | AATCCCTCCCCACGT[A/G]GGGATGAGAACCTTC | 57799 |
| rs115937591 | snp | C/T | 0.0539704 | 0.155153 | intron-variant | RAB40C | GRCh38.p7 | 16:591209 | GGAAGGTGTCATGGT[C/T]TGGGATCTCAGGGGA | 57799 |
| rs116141445 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | RAB40C | GRCh38.p7 | 16:622484 | GAGCGCGCGTCCTGA[C/G]TCATCCCCTAGAGCA | 57799 |
| rs116257690 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | RAB40C | GRCh38.p7 | 16:601065 | CCTCCTGGTCATTAG[C/T]GTTAAAGCTCTTCTC | 57799 |
| rs116262571 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | RAB40C | GRCh38.p7 | 16:620371 | GCACGCCAACCTGGG[C/T]GACGAGTGAAACTCC | 57799 |
| rs116567715 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RAB40C | GRCh38.p7 | 16:601066 | CTCCTGGTCATTAGC[A/G]TTAAAGCTCTTCTCT | 57799 |
| rs116606022 | snp | G/T | 0.081446 | 0.184634 | intron-variant, upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:589898 | GCGACCTCTGGTGAC[G/T]ACGGGAAGGCAGGGC | 57799 |
| rs116767363 | snp | C/G | 0.0599851 | 0.162463 | intron-variant | RAB40C | GRCh38.p7 | 16:625281 | GGCTGCACCAGCTCT[C/G]CCTGGAGGGCATGGC | 57799 |
| rs116903146 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593894 | TGCCCCTGGGTGATG[A/G]TGGCGAGTTACCCGG | 57799 |
| rs116908261 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RAB40C | GRCh38.p7 | 16:624060 | CTTCAGCATCTGCAC[C/G]GTACATTTCACTGCC | 57799 |
| rs116986963 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | RAB40C | GRCh38.p7 | 16:622243 | AAAAAAAGGTGTAAA[C/T]GTGCTCAGATGCATA | 57799 |
| rs116989993 | snp | C/T | 0.0479149 | 0.147179 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588951 | ACGTGCCCACTCAAC[C/T]CCCGACCCCACGCCG | 57799 |
| rs117109351 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | RAB40C | GRCh38.p7 | 16:622991 | TCATTTGGGTCCCTG[C/T]GGCCTCACTGTGACC | 57799 |
| rs117112974 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594040 | CGTGTTGGCCCCCAG[A/G]AACCACCCGCACAGG | 57799 |
| rs117218408 | snp | A/C/T | 0.00835779 | 0.0641761 | intron-variant | RAB40C | GRCh38.p7 | 16:617457 | CTGGGACACTGTGTC[A/C/T]CTAGAGATCGCGGCT | 57799 |
| rs117287956 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | RAB40C | GRCh38.p7 | 16:606624 | TGGGAGGTTGGCAGA[A/G]TTCCGTTCTTGCTGG | 57799 |
| rs117411093 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:591134 | CGAGGGAAGGTGTCA[C/T]AGATCTGGGGAAAGG | 57799 |
| rs117503696 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RAB40C | GRCh38.p7 | 16:623060 | CCCCTGCCCGTAACC[C/T]CTACTCCTCAGACAT | 57799 |
| rs117545065 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | RAB40C | GRCh38.p7 | 16:625158 | CCCAGGAAACTTCCA[C/T]AGGCTGATGGCTCCA | 57799 |
| rs117546158 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:608400 | TTATCACTCCTGAGC[C/G]TGCTTAGCTCCCACC | 57799 |
| rs117605911 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | RAB40C | GRCh38.p7 | 16:622478 | CAGGGCGAGCGCGCG[C/T]CCTGACTCATCCCCT | 57799 |
| rs117691034 | snp | A/C/G | 0.00636936 | 0.0560724 | intron-variant | RAB40C | GRCh38.p7 | 16:604649 | TCTGAAGGTGTTTCT[A/C/G]TTCCCTTAGGTAGAT | 57799 |
| rs117736707 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:613963 | GGGAAGCACACAGTC[A/G]GCGCAGATGCTTCCA | 57799 |
| rs117745787 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | RAB40C | GRCh38.p7 | 16:604349 | AACACAAATACGCAC[A/G]AGGCCTTCTGAAGGT | 57799 |
| rs117847554 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | RAB40C | GRCh38.p7 | 16:609172 | TTGATGGTTTGGGAA[C/T]AGCGGTGCTGCCACG | 57799 |
| rs117864333 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RAB40C | GRCh38.p7 | 16:611572 | GCCTCCCTGAAGAGT[A/G]TTGTTTCACTTGTGA | 57799 |
| rs117872096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:626231 | GTTCAGGCAGGTCCC[C/T]TGGCAACGCGCAGTA | 57799 |
| rs117876257 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593012 | AGAGGAGAGTCCACT[C/T]TTAGAAAGACACCAC | 57799 |
| rs117918714 | snp | A/T | 0.0178098 | 0.0926698 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587743 | TTTGTTTTTCTTTTT[A/T]AAAAAAGTTTATTTT | 57799 |
| rs117940568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:625570 | GGAGGTACCTGGGCC[C/T]CGGGTAGGCTCTGGA | 57799 |
| rs117996073 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | RAB40C | GRCh38.p7 | 16:621919 | TCGGCACACAGGTGG[A/G]CGGGTGGATGTGAGT | 57799 |
| rs118028349 | snp | C/T | 0.0309054 | 0.120406 | intron-variant | RAB40C | GRCh38.p7 | 16:617177 | GCTCCAGGAGTGGCG[C/T]GTCCCCTCAGCGCCC | 57799 |
| rs118041986 | snp | A/G/T | 0.0165278 | 0.0893908 | intron-variant | RAB40C | GRCh38.p7 | 16:608418 | CTTAGCTCCCACCTC[A/G/T]TCCTCTGTCCTTTTT | 57799 |
| rs118101930 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RAB40C | GRCh38.p7 | 16:603516 | CATCTGGCTCTGATA[C/T]GTGTTCAGGCTGTCT | 57799 |
| rs118186438 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | RAB40C | GRCh38.p7 | 16:601438 | GGGTCGCCAGGATCC[A/G]GCTCAGAGTGTGAGT | 57799 |
| rs137994755 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596233 | GGAAGGAAGCCACAT[A/C]GGGGAGCTGAGAGGT | 57799 |
| rs138290883 | snp | A/G/T | 0.0023933 | 0.0345097 | intron-variant | RAB40C | GRCh38.p7 | 16:625713 | AAGACCAGGAGCTAC[A/G/T]GGGCCACCCGGAAGG | 57799 |
| rs138383542 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | RAB40C | GRCh38.p7 | 16:606484 | CCTGAGCTGAAGTCA[A/G]GGTGTTGGCTGACAC | 57799 |
| rs138429744 | snp | G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:614580 | CTGCCTAACTCTACC[G/T]CATCCCGATGGTGAA | 57799 |
| rs138448913 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:615072 | GACCATCCGTCCATC[A/C]TAAAATTGGGACGTT | 57799 |
| rs138456803 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RAB40C | GRCh38.p7 | 16:602214 | AAATAATTGTGGAAT[A/G]AAATATATGACAACA | 57799 |
| rs138501561 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | RAB40C | GRCh38.p7 | 16:591744 | CTACAGGTGTATGCC[A/T]CCACGCCCGGCTAAT | 57799 |
| rs138514013 | in-del | -/TTTG | 0.177182 | 0.23916 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587728 | TGGAGAGCGTTTTAC[-/TTTG]GTTTTTCTTTTTTAA | 57799 |
| rs138640042 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:610325 | AGGCAGCGCCTGGCT[A/G]GGGCTAGATGAACAA | 57799 |
| rs138695547 | snp | A/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:607517 | AAAAAAAAAAAAAAA[A/C]GGGGGGCCGGGCGCG | 57799 |
| rs138700314 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:591531 | CAACGCTTTGTGCTA[A/G]AAGAAAATACCTCTG | 57799 |
| rs138736579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:602528 | ACGTCTGCCTCCTGG[A/G]TTCAAGCCTCTTGCC | 57799 |
| rs138746680 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:622474 | AGAGCAGGGCGAGCG[C/T]GCGTCCTGACTCATC | 57799 |
| rs138793109 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | RAB40C | GRCh38.p7 | 16:622919 | GGGTGCTTAGGGTGC[C/T]GTTCGTTAGGCGGCT | 57799 |
| rs138855752 | snp | C/T | 3.34773e-05 | 0.00409115 | stop-gained | RAB40C | GRCh38.p7 | 16:626118 | ATCTGGAGGCCCAAC[C/T]GAGGTGGGTGGGCGG | 57799 |
| rs138905192 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RAB40C | GRCh38.p7 | 16:599270 | GCTTTGCTCCGAGGG[A/G]TGTCTGTGTCCTCAG | 57799 |
| rs139128797 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RAB40C | GRCh38.p7 | 16:611059 | AATCCTGTTCTGACG[C/T]GCACCGTGGGCAACC | 57799 |
| rs139129905 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628179 | TTGGGTGACCGGGGC[C/T]CTGGCTCCCACGGGA | 57799 |
| rs139166605 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:609910 | ATGTGTCTCCAGACT[G/T]CAAGGGCCACAGAGT | 57799 |
| rs139179644 | in-del | -/A | 0.0383715 | 0.133092 | intron-variant | RAB40C | GRCh38.p7 | 16:621416 | CTGCCTCCCTCCGTT[-/A]GAGAGTGGAGAGGCC | 57799 |
| rs139197120 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | RAB40C | GRCh38.p7 | 16:608370 | GTGAGATTTGGGCGG[G/T]GACACAGCCAAATCT | 57799 |
| rs139211273 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RAB40C | GRCh38.p7 | 16:604459 | ATATATGTGAGTCCT[A/T]CTGAAGGTGTTTCTC | 57799 |
| rs139280562 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:620124 | GTTGGGGCTGGTGCG[C/G]TGGTTCACGCCTGTA | 57799 |
| rs139290838 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | RAB40C | GRCh38.p7 | 16:625482 | GTCCTTTGACGGCAT[C/T]GACCGCTGGATCAAG | 57799 |
| rs139397924 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RAB40C | GRCh38.p7 | 16:613546 | CTGCGAGGCTGGATC[A/G]TGGTGCGGTGGTGGC | 57799 |
| rs139415632 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:620895 | TCTGTGGGACACGAG[C/G]CCAGTACAGTCGTGA | 57799 |
| rs139551643 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RAB40C | GRCh38.p7 | 16:600479 | TGGTGCCGGATGGGC[A/G]CGGTGGCTCACGCCT | 57799 |
| rs139614950 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593318 | GACTCAGCATCTTGA[G/T]AATTTATTCTCCTTT | 57799 |
| rs139630998 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RAB40C | GRCh38.p7 | 16:623167 | CTTGGAGCCTGAGGC[A/G]GCCCATCAGCCGGGA | 57799 |
| rs139759290 | in-del | -/TA | 0.249038 | 0.249998 | intron-variant | RAB40C | GRCh38.p7 | 16:600440 | AGTTTAAAACATTGT[-/TA]TTGTTGGACTTTTTT | 57799 |
| rs139762254 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RAB40C | GRCh38.p7 | 16:603544 | TCTTGTAGGGTAATC[C/T]GGTCCCCTAATCCTT | 57799 |
| rs139778389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:597532 | TCCGTTACCCAGGGT[A/G]TAGTTCGATGGCACT | 57799 |
| rs139779459 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:600783 | GAGCTTTGGTGCCTA[C/T]GTGCGTCACACAGAC | 57799 |
| rs139898602 | snp | C/T | 3.36678e-05 | 0.00410277 | synonymous-codon | RAB40C | GRCh38.p7 | 16:627562 | CAAGAGGTCCAAGTC[C/T]ATCCGTCCACCCCAG | 57799 |
| rs139992748 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:592220 | CCGTCCTGTCTGACT[G/T]CCCTGAGCGTCTGCT | 57799 |
| rs140064450 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:621233 | GAGCATTTGGGCCAC[C/G]CCGGGAGCCCAGCCC | 57799 |
| rs140114947 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | RAB40C | GRCh38.p7 | 16:609334 | CAGACACCACTGGGG[A/T]TGGTGGGGGACAGGG | 57799 |
| rs140221729 | in-del | -/CTT | 0.0596104 | 0.162024 | cds-indel | RAB40C | GRCh38.p7 | 16:628337 | GCTGTGATGTGACAC[-/CTT]CGGGGACATTGACCA | 57799 |
| rs140243187 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:625685 | CACACGACAGTCGGG[C/T]GTGGAGCCCAGCAAG | 57799 |
| rs140420877 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RAB40C | GRCh38.p7 | 16:605781 | GTTTGGTCAACACAG[A/G]TGCCCATTGCTGTTG | 57799 |
| rs140616785 | snp | A/G | 0.0182019 | 0.0936463 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588453 | GATCGCTTGTGCCGG[A/G]GAGGTAGAGGCTGCA | 57799 |
| rs140650628 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RAB40C | GRCh38.p7 | 16:601960 | GTGAAACTCCGTCTC[C/T]ACTGAAAATATAAAA | 57799 |
| rs140707344 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | RAB40C | GRCh38.p7 | 16:599308 | CAAGGCAGTGTCAGG[C/G]TGATGCCTGCCCGTG | 57799 |
| rs140728271 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:614587 | ACTCTACCGCATCCC[A/G]ATGGTGAACTGCCTA | 57799 |
| rs140799238 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | RAB40C | GRCh38.p7 | 16:598954 | CTGCTTTCCCTGCCC[G/T]GGGCCGGCGGCTGCT | 57799 |
| rs140887455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594494 | GTGTCCCAGCTTCTT[C/T]GGCTTCACGACTCCC | 57799 |
| rs140930093 | in-del | -/C | 0.259397 | 0.249823 | intron-variant | RAB40C | GRCh38.p7 | 16:610363 | ATTGGGAACAGTAAA[-/C]CCTGAGGTGGTGAGC | 57799 |
| rs140977669 | in-del | -/CGT | 0.0569829 | 0.158885 | intron-variant | RAB40C | GRCh38.p7 | 16:622407 | GCGGCACCGTGGACA[-/CGT]CTGTAGACGCTGAGG | 57799 |
| rs141032788 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RAB40C | GRCh38.p7 | 16:615588 | TGTCGTGCCTGCGTT[A/G]AGTGTCCAGAACTGT | 57799 |
| rs141130105 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | RAB40C | GRCh38.p7 | 16:608326 | TATCTCCATCTGGCC[C/T]CGCCCTCAACCTGTG | 57799 |
| rs141157546 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:616948 | CTAGGCTGTGGGGCC[C/T]GATGGCCTGACACTG | 57799 |
| rs141183008 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:614611 | CTGCCTAACTCTACC[A/G]CATCCCGATGGTGAA | 57799 |
| rs141213566 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595852 | GTGATCCACCCTCCT[C/T]GGCCTCCCAAAGTGC | 57799 |
| rs141404679 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RAB40C | GRCh38.p7 | 16:605173 | GAGGCTGCAGCGAGC[C/T]GTGATTGTTCCGCTG | 57799 |
| rs141428975 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:601814 | TCCCTGCAAAAAAAA[A/G]TAAAAAAAAAAAAAA | 57799 |
| rs141469646 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | RAB40C | GRCh38.p7 | 16:602228 | TGAAATATATGACAA[C/T]ATTAGCAGTGGTCAT | 57799 |
| rs141603109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596693 | AGGGACCAGAAGTTA[C/T]GAAGGCGGTGGGAAG | 57799 |
| rs141711846 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RAB40C | GRCh38.p7 | 16:610060 | CCAGGCCAGGGCCAG[A/G]TGTAGCCTCATACCA | 57799 |
| rs141847125 | snp | A/G | 1.67203e-05 | 0.00289134 | missense | RAB40C | GRCh38.p7 | 16:625504 | TGGATCAAGGAGATC[A/G]ATGAGGTAGGCCTGG | 57799 |
| rs141907535 | snp | A/G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:627708 | GCCAGTGCCGCCTAC[A/G/T]TGGAGACTGTCCACA | 57799 |
| rs141913010 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:626424 | AGTGTGTGCTCGCTC[A/C]TTCCTGGTTCCGGGG | 57799 |
| rs141932842 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:624206 | GGGAGGTTGCCATGC[A/G]GGAGGTTGCCACTAG | 57799 |
| rs141954174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:591785 | GTATTTTAGTAGAGA[C/T]GGGGTTTCAGCATGT | 57799 |
| rs141954894 | in-del | -/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:611451 | TCATGGGGGCTTCAA[-/C]CAGCCAGGACCAAAA | 57799 |
| rs141976975 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | RAB40C | GRCh38.p7 | 16:622931 | TGCCGTTCGTTAGGC[A/G]GCTGCTGGTCACCGA | 57799 |
| rs142091223 | snp | A/G | 1.64982e-05 | 0.00287208 | missense | RAB40C | GRCh38.p7 | 16:627428 | CCACTGCCCGTCACC[A/G]TCAAGAGCCACCTCA | 57799 |
| rs142098590 | snp | C/G/T | 0.00251179 | 0.0353499 | missense, synonymous-codon | RAB40C | GRCh38.p7 | 16:617212 | CTTCCTCGCAGGGAT[C/G/T]GACTACAAGACCACC | 57799 |
| rs142133581 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RAB40C | GRCh38.p7 | 16:601738 | CCCAGCTACTTGGGA[A/G]GTCAAGGCAGGCGAT | 57799 |
| rs142169601 | snp | C/G | 1.72305e-05 | 0.00293513 | missense | RAB40C | GRCh38.p7 | 16:627585 | CACCCCAGAGCCCCC[C/G]CCAGAACTGCTCGCG | 57799 |
| rs142285305 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588213 | GAAACATCACATCTT[C/T]GGTGCTTCCCGTCCC | 57799 |
| rs142329137 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:614099 | CTGCCGAACTCTACC[A/G]CATCCCGATGGTGAA | 57799 |
| rs142398362 | snp | G/T | 0.0325976 | 0.123435 | intron-variant | RAB40C | GRCh38.p7 | 16:613294 | GACAGCTGCCCTTGC[G/T]TGTAGAATCAAGAGC | 57799 |
| rs142413104 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:609836 | TCACCCTGGCTGGCG[C/T]GGCTCAGGATGGAGG | 57799 |
| rs142609706 | in-del | -/CTT | 0.16976 | 0.236773 | intron-variant | RAB40C | GRCh38.p7 | 16:604492 | GAATACACGTGAGTC[-/CTT]TCTGAGGGTGTTTCT | 57799 |
| rs142627133 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594288 | GGGTTCAGTGTTGGT[A/G]GAAGCTGCTGAGTGA | 57799 |
| rs142716551 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RAB40C | GRCh38.p7 | 16:603567 | TAATCCTTAGACCTC[C/T]AAATTCAAAGCAGAT | 57799 |
| rs142729402 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:624090 | CGCTTACTCAGCTGT[C/T]CCCTGAGGCTGGACA | 57799 |
| rs142773446 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:591577 | CATTTGTTTTGTTTT[C/G]TTTTCTTTTCTTTTC | 57799 |
| rs142777614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:597335 | CCCTGAGCAGCCTTC[A/G]CCGTCTTTACAGTGA | 57799 |
| rs142783063 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:603376 | GTGGGGTTGGTGGAC[A/G]TGGGCTGTCCTTGTC | 57799 |
| rs142819617 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | RAB40C | GRCh38.p7 | 16:618099 | CTGTCCTGGCCGCCC[C/T]GCTCCCCTCAGGACA | 57799 |
| rs143304834 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:619342 | CATGTGTGTGTGCAG[C/G]CATGTGCACAGGTCT | 57799 |
| rs143345732 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | RAB40C | GRCh38.p7 | 16:617799 | AGTGAGCTGAGATTG[C/T]ACCACTGCACTCCAG | 57799 |
| rs143348269 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596452 | GCGCAGCACATGGTA[C/T]GATGCCACCCCACCG | 57799 |
| rs143376117 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | RAB40C | GRCh38.p7 | 16:605452 | GAAAGCATCAGCCCT[C/T]GCAGCCTCGCCCTCT | 57799 |
| rs143445250 | snp | A/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:601815 | CCCTGCAAAAAAAAG[A/T]AAAAAAAAAAAAAAA | 57799 |
| rs143452164 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RAB40C | GRCh38.p7 | 16:619727 | GGAAGGTTCAGGTCT[A/G]TGCCATGCAGCTTCT | 57799 |
| rs143577846 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | RAB40C | GRCh38.p7 | 16:619865 | TGTAGTCGGTGTTGG[A/G]TCTGATGTCTTCTAC | 57799 |
| rs143653331 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:609639 | AGATACCGCATCCAC[A/G]AATGAAGAGCCAGAC | 57799 |
| rs143729764 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:621289 | AGCAGCGGTGAGGTG[C/T]GGGTGCATCCAGCCG | 57799 |
| rs143786182 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RAB40C | GRCh38.p7 | 16:622506 | CCTAGAGCACTCGCT[C/T]GTTCTTTTGTTTTGT | 57799 |
| rs143953020 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | RAB40C | GRCh38.p7 | 16:617467 | GTGTCCCTAGAGATC[A/G]CGGCTCCCCTCCTGC | 57799 |
| rs144059335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:608587 | GAAAAGAATGAAACT[C/T]GGCTGGCCATGGTGG | 57799 |
| rs144083169 | in-del | -/T | 0.0119091 | 0.0762411 | intron-variant | RAB40C | GRCh38.p7 | 16:600214 | TGTCCTGGAACAGTC[-/T]GTACTTCCAGCAGAT | 57799 |
| rs144114998 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | RAB40C | GRCh38.p7 | 16:607988 | TCTGCAGCCAGGCAA[C/T]GTGCTGTGCCCGTCC | 57799 |
| rs144198679 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629557 | CCGGCAGCAGATGGC[C/G]TGGGGCGGACTGTCC | 57799 |
| rs144205704 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | RAB40C | GRCh38.p7 | 16:624575 | GGCTCTAAAAACCCT[A/T]ATTTTCAGATGGACA | 57799 |
| rs144226075 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587982 | CTGGCTCATTTTTGT[A/G]TTTTCAGTGGAGAGG | 57799 |
| rs144252473 | snp | C/T | 0.000681227 | 0.0184431 | synonymous-codon | RAB40C | GRCh38.p7 | 16:626090 | CGTGCTCATGCGGCA[C/T]GGCATGGAGAAGATC | 57799 |
| rs144322672 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593760 | TCTCCTAATGTGGGT[G/T]TGCGCTGGGTTTCTG | 57799 |
| rs144391427 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | RAB40C | GRCh38.p7 | 16:604665 | TTCCCTTAGGTAGAT[C/T]TAAGAGTGGAATTGC | 57799 |
| rs144435553 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | RAB40C | GRCh38.p7 | 16:600562 | TCAAGACCGTTCTGA[C/G]CAACATGGTGAAACC | 57799 |
| rs144611482 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | RAB40C | GRCh38.p7 | 16:615686 | TGTGATGTGGGCCGG[G/T]CACGGTGGCTCACAC | 57799 |
| rs144670488 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RAB40C | GRCh38.p7 | 16:618029 | GCTCAGCGGCACGGC[A/G]CCAGGCTGCTGTGAC | 57799 |
| rs144717195 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RAB40C | GRCh38.p7 | 16:602633 | AGATGAGGTTTCACC[A/G]TGTCGGCCAGGCTGG | 57799 |
| rs144776352 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:615268 | GTCAGGCAGAAGGAC[A/G]GTGTGGGTGGAAGCG | 57799 |
| rs144798661 | snp | C/G | 0.0119091 | 0.0762411 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588811 | CTTTTACTTACGACT[C/G]TAACAGCGCTACTGA | 57799 |
| rs144857040 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | RAB40C | GRCh38.p7 | 16:610086 | TACCAGCCCAGCTGG[C/G]AGTCCGCTTGCTGAG | 57799 |
| rs144921178 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RAB40C | GRCh38.p7 | 16:601034 | CATTTAGACCCTTAG[C/G]CTCCTTGCAGAGCCA | 57799 |
| rs145021288 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:600876 | AGAAAGGTTTTGACT[C/G]CAGTCTCTGTCTTCT | 57799 |
| rs145028658 | snp | C/T | 0.081446 | 0.184634 | intron-variant, downstream-variant-500B | RAB40C, LOC101929280 | GRCh38.p7 | 16:598203 | GCTAACATGGTGAAA[C/T]CCTGTCTCTATAAAA | 57799 |
| rs145033613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:598628 | ACGTCTGTAGTCCCA[A/G]TTACTTGGGAGGCTG | 57799 |
| rs145146569 | snp | C/T | 1.65732e-05 | 0.00287859 | synonymous-codon | RAB40C | GRCh38.p7 | 16:626042 | CCTGTGCAACTTCAA[C/T]GTCATCGAGTCCTTC | 57799 |
| rs145255564 | snp | C/T | 0.158962 | 0.232835 | intron-variant | RAB40C | GRCh38.p7 | 16:615886 | AGAATCGCTTGAACC[C/T]GGGAGGTGGAGGTTG | 57799 |
| rs145462058 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | RAB40C | GRCh38.p7 | 16:616393 | ACCCAGGCAGGAGTG[C/T]AGTGACATGATCTCG | 57799 |
| rs145488924 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | RAB40C | GRCh38.p7 | 16:604280 | AAAATACAGAAAACA[C/T]GTCATTTTAGCCATA | 57799 |
| rs145581890 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | RAB40C | GRCh38.p7 | 16:615439 | TGTTTAAAAAGTGCC[C/T]GTTTCCAAGCCCCTT | 57799 |
| rs145637964 | snp | A/T | | | missense | RAB40C | GRCh38.p7 | 16:590329 | TGAAGAGCTACGACT[A/T]CCTGCTCAAGTTCCT | 57799 |
| rs145695945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:613584 | GGTTTCTCTGCTGAA[C/T]GATGATGTGGAATGC | 57799 |
| rs145757340 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594502 | GCTTCTTCGGCTTCA[C/T]GACTCCCTGAGCTTT | 57799 |
| rs145769634 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | RAB40C | GRCh38.p7 | 16:590923 | GAAGGTGTCATAGGT[C/G]CGAGGGAAGGTGTCA | 57799 |
| rs145837399 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | RAB40C | GRCh38.p7 | 16:622469 | GGCCTAGAGCAGGGC[A/G]AGCGCGCGTCCTGAC | 57799 |
| rs145844236 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RAB40C | GRCh38.p7 | 16:609576 | GGAAAGACCCAGACA[A/G]GCAGGAAAAGAGCTC | 57799 |
| rs145862810 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | RAB40C | GRCh38.p7 | 16:599454 | AGGAGGAGGCAGCTT[C/T]CCTTGGGGCCACGCC | 57799 |
| rs145951340 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:615002 | CTGCTCACAGCCGTG[A/G]CCCTTTTGGCACAAC | 57799 |
| rs145997805 | snp | A/G | 0.000132877 | 0.0081499 | missense | RAB40C | GRCh38.p7 | 16:627527 | GGGGCCGGGGGCGGC[A/G]GCAGCAAGGGCAACA | 57799 |
| rs146176560 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:610948 | GACACTCGGCTGACT[A/G]TGCTTAGAGAACAGG | 57799 |
| rs146195336 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RAB40C | GRCh38.p7 | 16:608330 | TCCATCTGGCCCCGC[C/T]CTCAACCTGTGGGGA | 57799 |
| rs146222221 | snp | G/T | 0.264084 | 0.249603 | intron-variant | RAB40C | GRCh38.p7 | 16:614179 | CGATGGTGAACTGCC[G/T]AACTCTACCGCATCC | 57799 |
| rs146294753 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596904 | GGGATGGCGGCGCAC[C/T]CTGATACAGGCAGTG | 57799 |
| rs146315444 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RAB40C | GRCh38.p7 | 16:626465 | TGTCAGGGGAGCACA[A/G]GAGCCGTGCCTGCAG | 57799 |
| rs146315547 | snp | A/G | 0.0146672 | 0.084371 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593090 | GTGGCCTCGAGCAGA[A/G]AAGGAAGCGCCTCTG | 57799 |
| rs146317318 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RAB40C | GRCh38.p7 | 16:623044 | TCCTCCTGTGCCATC[A/G]CCCCTGCCCGTAACC | 57799 |
| rs146602754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:609187 | CAGCGGTGCTGCCAC[A/G]GCTGGGTGAGGGGCC | 57799 |
| rs146620489 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:605164 | CTGGAGTTGGAGGCT[A/G]CAGCGAGCCGTGATT | 57799 |
| rs146656939 | in-del | -/CAGCCCC | | | intron-variant | RAB40C | GRCh38.p7 | 16:603773 | CAGGCCCTGCCGAGT[-/CAGCCCC]CAGCCCCCAGCCCCC | 57799 |
| rs146668461 | in-del | -/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:614177 | CCCGATGGTGAACTG[-/C]CCGAACTCTACCGCA | 57799 |
| rs146714041 | snp | C/T | 0.000153988 | 0.00877328 | missense | RAB40C | GRCh38.p7 | 16:617223 | GGATCGACTACAAGA[C/T]CACCACCATCCTGCT | 57799 |
| rs146720565 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594033 | GTGGGCCCGTGTTGG[A/C]CCCCAGGAACCACCC | 57799 |
| rs146803585 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588255 | GCCTCAGGGACTTCA[C/T]AGCCAGGGCTCAAGT | 57799 |
| rs146820700 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:621290 | GCAGCGGTGAGGTGC[A/G]GGTGCATCCAGCCGA | 57799 |
| rs146948578 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595969 | GGAAACTGTTGAGTC[A/G]GTAGGTAGAATATTG | 57799 |
| rs146977233 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:607484 | CTCCGGCCTGGACAA[C/T]GAGAGTGAAACTGTC | 57799 |
| rs147082787 | snp | C/G | 0.021333 | 0.101051 | intron-variant | RAB40C | GRCh38.p7 | 16:591582 | GTTTTGTTTTGTTTT[C/G]TTTTCTTTTCTTTCT | 57799 |
| rs147206638 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628677 | CCAGGCACGCAGGGC[C/T]GGCCACCTCTCTCCT | 57799 |
| rs147296229 | in-del | -/G | 0.0150905 | 0.0855425 | intron-variant | RAB40C | GRCh38.p7 | 16:590752 | GGGATCTGGAGCCCA[-/G]GGGAAGGTGTCATGG | 57799 |
| rs147310413 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:617485 | GCTCCCCTCCTGCCC[C/T]GGAAAACCTGATTCC | 57799 |
| rs147313965 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RAB40C | GRCh38.p7 | 16:615519 | GGGAAGGGGCTGAGC[C/T]CTAAAGGTAGAAGCT | 57799 |
| rs147476445 | in-del | -/GG | | | intron-variant | RAB40C | GRCh38.p7 | 16:602262 | TGTTTTTTTTTTTTT[-/GG]TTTTGTTTTTTTTTA | 57799 |
| rs147512714 | snp | C/T | 0.0103295 | 0.0711199 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587525 | TGGGAGGTCAGAGGG[C/T]ACAGCAGCTTTCCAA | 57799 |
| rs147570330 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | RAB40C | GRCh38.p7 | 16:622284 | TACCCAAGAGCTGGC[A/G]CAGTACCAGTTCACG | 57799 |
| rs147645802 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | RAB40C | GRCh38.p7 | 16:624127 | TTGTGTCTGGCTTGT[C/G]GTTGTTATCAGCGCC | 57799 |
| rs147674090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:609835 | GTCACCCTGGCTGGC[A/G]CGGCTCAGGATGGAG | 57799 |
| rs147748665 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | RAB40C | GRCh38.p7 | 16:614094 | GTGAACTGCCGAACT[C/G]TACCGCATCCCGATG | 57799 |
| rs147778929 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595148 | GGTTTTCCAGCAGGG[A/T]GGTGTTGTGGGAGGA | 57799 |
| rs147864861 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:614491 | ACTGCTAACTCTGCC[A/G]CATCCCGATGGTGAA | 57799 |
| rs148005662 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RAB40C | GRCh38.p7 | 16:619829 | ATGGCAAGCTCATTT[C/T]CTTCCATTTCTACAC | 57799 |
| rs148166073 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | RAB40C | GRCh38.p7 | 16:622598 | CTGCAACCTCCGCCT[C/T]CCGGGTTCACGCCAT | 57799 |
| rs148202374 | snp | A/G/T | 0.0111301 | 0.0738707 | intron-variant | RAB40C | GRCh38.p7 | 16:616835 | CCCTGCCTTTGCCCA[A/G/T]TGCCCTCTGAGGGAG | 57799 |
| rs148322334 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:599647 | TGGCATTAATCAGCG[C/T]GGATTCAGCAAGGTT | 57799 |
| rs148375032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596604 | TGAGAAGGCGGGGAG[A/G]CTGCTTGTCAGGCTG | 57799 |
| rs148473224 | in-del | -/T | 0.0295035 | 0.117819 | intron-variant | RAB40C | GRCh38.p7 | 16:603298 | CAGACACATTTGAAA[-/T]TTTGTTAGATAACTT | 57799 |
| rs148476578 | snp | C/T | 0.179744 | 0.239925 | intron-variant | RAB40C | GRCh38.p7 | 16:623454 | GGAGATCAAGACCAT[C/T]CTGGCTAACACGGTG | 57799 |
| rs148481780 | in-del | -/GGCC | | | intron-variant | RAB40C | GRCh38.p7 | 16:610961 | TGTGCTTAGAGAACA[-/GGCC]GGCCGCTGTTTGTGT | 57799 |
| rs148499099 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:618094 | GGCACCTGTCCTGGC[C/T]GCCCCGCTCCCCTCA | 57799 |
| rs148517769 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:614582 | GCCTAACTCTACCGC[A/G]TCCCGATGGTGAACT | 57799 |
| rs148550288 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | RAB40C | GRCh38.p7 | 16:615305 | CCTGAAGAAGGGCAC[C/T]GTAGGCAGAGAGACC | 57799 |
| rs148640239 | snp | A/G/T | 0.108048 | 0.20579 | intron-variant | RAB40C | GRCh38.p7 | 16:613218 | TCAGCAGGGACAGCC[A/G/T]CCCTGGCCTGTAGCA | 57799 |
| rs148654560 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:614347 | AACTCTGCCGCATCC[C/T]GATGGTGAACTGCCA | 57799 |
| rs148689826 | snp | A/G | 0.0221141 | 0.102801 | intron-variant, downstream-variant-500B | RAB40C, LOC101929280 | GRCh38.p7 | 16:598402 | AAAAATACAAATACA[A/G]ATACAAAAATTAGCC | 57799 |
| rs148692024 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:608170 | AATTTACAGTCATGG[C/T]GGAAGGTACCTCACA | 57799 |
| rs148708515 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587999 | TTTCAGTGGAGAGGG[A/G]GTTATCACGATGTTG | 57799 |
| rs148812297 | snp | C/T | 0.000543055 | 0.0164691 | synonymous-codon | RAB40C | GRCh38.p7 | 16:590330 | GAAGAGCTACGACTA[C/T]CTGCTCAAGTTCCTG | 57799 |
| rs148864190 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | RAB40C | GRCh38.p7 | 16:616181 | TAATGGCGTGAACCC[A/G]GGAGACGGAGCTTGC | 57799 |
| rs149017137 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:609631 | GTCATCAGAGATACC[A/G]CATCCACGAATGAAG | 57799 |
| rs149025351 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:590590 | CTCGGTGGCTGCGGG[A/G/T]TGCCCGTGCTCCAGT | 57799 |
| rs149052663 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | RAB40C | GRCh38.p7 | 16:601221 | AAACTATGATTTTTT[G/T]TGTGTTATCCACACC | 57799 |
| rs149195145 | snp | A/C/G | 0.0140236 | 0.082555 | synonymous-codon | RAB40C | GRCh38.p7 | 16:625985 | GGAGCAGGCCCGCGC[A/C/G]TACGCAGAGAAGAAC | 57799 |
| rs149278187 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:615185 | TCCATCTCTGGGTTG[C/T]ATTTTTCTGTCCATT | 57799 |
| rs149336685 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | RAB40C | GRCh38.p7 | 16:610493 | GACCTTCACTGGCGC[A/C]CTTGCCTTTTCACTG | 57799 |
| rs149340448 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | RAB40C | GRCh38.p7 | 16:592845 | TGGAGAGACAGGACC[C/G]TCCTTCCTCCCTGTC | 57799 |
| rs149515018 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:607883 | ACCTAGTAAAGCAAA[C/T]GCCTCAGTGACATTT | 57799 |
| rs149553764 | snp | C/T | 0.000381265 | 0.0138017 | missense | RAB40C | GRCh38.p7 | 16:626059 | TCATCGAGTCCTTCA[C/T]GGAGCTATCCCGCAT | 57799 |
| rs149560152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:621007 | CAAGCTCTGTTATCA[C/T]CTCCGTGTTCTTTCC | 57799 |
| rs149602910 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596268 | GGGAAGGACACAAGG[C/G]AGGGATCTGGGTCCT | 57799 |
| rs149672947 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | RAB40C | GRCh38.p7 | 16:604200 | GCTGGGACTACAGGC[A/G]TGTACCACCACACCC | 57799 |
| rs149756733 | snp | A/G | 1.98116e-05 | 0.00314728 | synonymous-codon | RAB40C | GRCh38.p7 | 16:590312 | CTCGCAGGGCAGTCC[A/G]GTGAAGAGCTACGAC | 57799 |
| rs149825765 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RAB40C | GRCh38.p7 | 16:609403 | CCTGGGAACTCAGGG[C/T]CTCCTGATATGCAGA | 57799 |
| rs149979574 | in-del | -/CTT | 0.0023933 | 0.0345097 | intron-variant | RAB40C | GRCh38.p7 | 16:606784 | CATGCTTTGACTCTC[-/CTT]CTGTCTCATCTGTAG | 57799 |
| rs150018864 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | RAB40C | GRCh38.p7 | 16:615877 | TGAGGCAGGAGAATC[A/G]CTTGAACCCGGGAGG | 57799 |
| rs150069140 | snp | A/C | 0.00517822 | 0.0506191 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587854 | ACTCTGTAGCCCAGG[A/C]TGGAGTGCAGTGGCA | 57799 |
| rs150192462 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:602298 | AGAGACAGTTTCACT[A/C]TTCCAGGCTGGAGTG | 57799 |
| rs150245124 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | RAB40C | GRCh38.p7 | 16:599255 | CTGCCTGTGCCACCA[A/G]CTTTGCTCCGAGGGG | 57799 |
| rs150296815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:622107 | AAATGTTCAAACCTC[A/G]GATCTTTGTATTTTG | 57799 |
| rs150384847 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:589717 | ATGATCTTGGTGAAC[C/T]TATAATCGAACCAAT | 57799 |
| rs150471824 | snp | A/G | 6.73129e-05 | 0.00580103 | synonymous-codon | RAB40C | GRCh38.p7 | 16:625967 | CAAGCGGCAGGTCCC[A/G]ACGGAGCAGGCCCGC | 57799 |
| rs150506239 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | RAB40C | GRCh38.p7 | 16:604042 | TGCTGATGTGAACGA[A/G]TTCTTCTTTTTTCTT | 57799 |
| rs150610668 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RAB40C | GRCh38.p7 | 16:622804 | CCACGGCGCCTGGCC[A/G]AAGTCGCTAGTTTTT | 57799 |
| rs150686065 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:592062 | GACCCAGCCGAATGG[C/G]ATGTGGCCCCAGATG | 57799 |
| rs150768098 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:627740 | AGCTGCCTCAGAAGC[A/G]CCGGGCTTTCCTCAC | 57799 |
| rs150789883 | snp | A/C/G | 0.000155544 | 0.0088177 | missense | RAB40C | GRCh38.p7 | 16:627587 | CCCCAGAGCCCCCCC[A/C/G]AGAACTGCTCGCGGA | 57799 |
| rs150794581 | in-del | -/AGCACAA | 0.0174175 | 0.0916809 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593157 | GGTTAAGACGTGCAC[-/AGCACAA]GGAGCAGGTCTTTGT | 57799 |
| rs150890093 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | RAB40C | GRCh38.p7 | 16:613431 | ACTGCCGCCCTGGCC[G/T]GTAGAATCAAGAGCA | 57799 |
| rs150947390 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RAB40C | GRCh38.p7 | 16:598916 | GCTCCAGCAGCGTGG[A/G]TAACCCGGTGGGAGC | 57799 |
| rs151164567 | in-del | -/C | 0.0150606 | 0.0854603 | intron-variant | RAB40C | GRCh38.p7 | 16:626544 | GAGGCTCCCGTGAAG[-/C]CCCCCTCAGGGAGGT | 57799 |
| rs151174150 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RAB40C | GRCh38.p7 | 16:601954 | AGCATGGTGAAACTC[C/T]GTCTCTACTGAAAAT | 57799 |
| rs151211957 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | RAB40C | GRCh38.p7 | 16:621914 | GCTTGTCGGCACACA[C/G]GTGGGCGGGTGGATG | 57799 |
| rs151331658 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RAB40C | GRCh38.p7 | 16:605646 | TGCTCCCTCCTTCCC[C/T]GCGCCGAGTGGTCTC | 57799 |
| rs180980242 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RAB40C | GRCh38.p7 | 16:604425 | AATACACGAGTCCTT[A/C]TGAAGGTGTTTCTCT | 57799 |
| rs181055164 | snp | A/C/G | 0.000285495 | 0.0119446 | intron-variant | RAB40C | GRCh38.p7 | 16:626125 | GGCCCAACCGAGGTG[A/C/G]GTGGGCGGGCGCCGG | 57799 |
| rs181094787 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | RAB40C | GRCh38.p7 | 16:610285 | GTGCCGTGTGTCTCA[G/T]GGGGTTGTGTTCAGG | 57799 |
| rs181171423 | snp | A/G | 0.00401605 | 0.0446307 | intron-variant | RAB40C | GRCh38.p7 | 16:590748 | CGGGATCTGGAGCCC[A/G]GGGGAAGGTGTCATG | 57799 |
| rs181241385 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RAB40C | GRCh38.p7 | 16:605574 | AAACTCTCCTGTGTC[C/T]GGCTGCCTTCTTTCC | 57799 |
| rs181245065 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | RAB40C | GRCh38.p7 | 16:626325 | CTGGGGGGCACAGGA[A/G]CAGCTGATGACCCCC | 57799 |
| rs181297683 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594589 | TGGCCAATTCCAGGG[C/G]ACACTATCTTGAGAG | 57799 |
| rs181399846 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:615576 | GCCTGTTTAAGATGT[C/T]GTGCCTGCGTTAAGT | 57799 |
| rs181710803 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:598542 | CTCCAGCTTGGTGAC[A/C]GAGCGAGACTCTGTC | 57799 |
| rs181721021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:620892 | AGGTCTGTGGGACAC[A/G]AGGCCAGTACAGTCG | 57799 |
| rs181837286 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595071 | TGATCCACCTGCCTC[A/G]GGGGTTTTGCTCGTT | 57799 |
| rs181841218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:616028 | TTTGGGAGGCTGAGG[C/T]GGGTGGATCATGAGG | 57799 |
| rs181885357 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | RAB40C | GRCh38.p7 | 16:611361 | CCACATTGGCACGTC[C/G]AGGTGACCGTCAAGG | 57799 |
| rs181886599 | snp | A/G | | | intron-variant, utr-variant-5-prime | RAB40C | GRCh38.p7 | 16:590192 | GCCGCCGTGGGGCGG[A/G]CGCAACGGGCGCAGG | 57799 |
| rs181892412 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629736 | GCACTCCAGTTGGTA[C/T]AGGGACCAGACCACA | 57799 |
| rs181893988 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | RAB40C | GRCh38.p7 | 16:608645 | GAGGCCGAGGCAGGC[A/C]GATCACTTGAGGTCA | 57799 |
| rs181994404 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:624936 | CCCGTGGCAAAACCT[G/T]CTCTGCCTGGCTGGG | 57799 |
| rs182096370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:626959 | AAACAAAAGAATGAG[C/T]GAGTGCTCTAGGGAA | 57799 |
| rs182100122 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:606862 | CACCCAGATAATCCC[A/G]GATAATCTCCCACCT | 57799 |
| rs182157977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:591184 | CAGGGGAAGGTGTCA[C/T]GGGCCTAAGGGAAGG | 57799 |
| rs182160246 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RAB40C | GRCh38.p7 | 16:599470 | CCTTGGGGCCACGCC[G/T]TGCCTCCTCCGTGTG | 57799 |
| rs182265558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:604311 | TGTAGGGATACAGTT[C/T]AGTGGCACTAGCACT | 57799 |
| rs182434357 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | RAB40C | GRCh38.p7 | 16:621449 | GAAGGTCCCCGCGGC[C/G]TGGGTCTTGCAGATG | 57799 |
| rs182447100 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:600523 | TTTGGGAGGCCGAGG[C/T]GGGCGGATCACAAGG | 57799 |
| rs182749664 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:616709 | TGGGCTGCAGTAAGC[C/T]GAGACTTGGAAATAC | 57799 |
| rs182908880 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:622385 | TGACCCCGCCCGCGA[A/G]GCATGAGCGGCACCG | 57799 |
| rs182917823 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:592290 | GCGCAGCATCCCCCA[A/C]TCTCTCAACTCGGGG | 57799 |
| rs183027807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596015 | CAGAGGCCAGATGCC[A/G]GAACTTTTGGACAAG | 57799 |
| rs183055760 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596606 | AGAAGGCGGGGAGAC[G/T]GCTTGTCAGGCTGAG | 57799 |
| rs183058336 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:601232 | TTTTGTGTGTTATCC[A/C]CACCATCAAGGCTGT | 57799 |
| rs183176216 | snp | A/G | 0.00795532 | 0.062565 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:597438 | ACCCTGATGAAAGAC[A/G]TGCCCATCCTGTGAG | 57799 |
| rs183195671 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RAB40C | GRCh38.p7 | 16:613620 | CACTGCTTCTTGGTC[A/G]TCGGTTTTTCTTCTT | 57799 |
| rs183244796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:614037 | ACTGCCTAACTCTAC[C/T]GCGTCCCGATGGTGA | 57799 |
| rs183342387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:617692 | TACTAAAAATACAAA[A/G]ATTAGCCAGGTGTGG | 57799 |
| rs183404360 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | RAB40C | GRCh38.p7 | 16:591702 | GTTCAAGCGATTCCC[C/G]TGTCTCAGCCTCCCG | 57799 |
| rs183443743 | snp | A/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:612684 | TGCCCTGGCCTGTAG[A/C]ATCAAGAGCAAGGGA | 57799 |
| rs183476305 | snp | A/T | 0.00849914 | 0.0646323 | intron-variant | RAB40C | GRCh38.p7 | 16:590459 | GCCCGCGGCGCGCGC[A/T]GCTACGCGGGGCCCG | 57799 |
| rs183495468 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:609486 | GCCACGAGACGCCGC[C/T]GAGAGCCCCAACTTA | 57799 |
| rs183806600 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:626694 | TGTAATCCCAGCACT[C/T]TGGGAGGCCACAGCA | 57799 |
| rs183948483 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:602034 | AGGAGGCTGAGGCAA[A/G]AGAATCGCTTCAACC | 57799 |
| rs183971627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:605927 | TCTAAGTCCTGCCTT[C/T]CTTTTAGCCATGCTG | 57799 |
| rs184108756 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:602825 | TTCTCTCACCTTGGC[A/C]TCCCAAAGTGTCGAG | 57799 |
| rs184116083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:624037 | GCTTTTACATGCACT[A/G]CTGCTGTCTTCAGCA | 57799 |
| rs184127537 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:623394 | GTGGCTCACGCCTGT[A/C]ATCCCAGCACTTTGG | 57799 |
| rs184137749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:620056 | GCAGGCAGGTGGAAG[A/G]CGGGCAGGCTCAAGG | 57799 |
| rs184247945 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:607928 | CCCCCTCCACTGCCC[A/G]TTTTCAGATTGATGC | 57799 |
| rs184258505 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | RAB40C, LOC101929280 | GRCh38.p7 | 16:598430 | GCCGGGCGTGGTGGC[A/G]CATACCTGTAGCCCC | 57799 |
| rs184264485 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628044 | GGGGACGCACTTGGG[A/G]CTCCTCGAGAGGGGA | 57799 |
| rs184272395 | snp | A/G | | | intron-variant, downstream-variant-500B | RAB40C, LOC101929280 | GRCh38.p7 | 16:597975 | AAAAAGGCCGGGTGC[A/G]GTGGCTCACACCTGT | 57799 |
| rs184379474 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:603955 | TTTGCACAAATATAC[A/C]CCAGTTTGTTTATGC | 57799 |
| rs184384355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:624882 | CAGCCCAGAGCTGAG[C/T]TCCAAGTAATTGGTC | 57799 |
| rs184722105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594266 | TATTTCTCTCTCTGC[C/T]CTTTTGGGGTTCAGT | 57799 |
| rs184771628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593521 | GTGCAAGGCTTACTG[C/T]TTCAGCATGGCCCAC | 57799 |
| rs184852356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:614998 | TGGGCTGCTCACAGC[C/T]GTGGCCCTTTTGGCA | 57799 |
| rs184951178 | snp | C/T | 0.00279162 | 0.0372561 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588143 | CAGGAAAGGAGGAGA[C/T]GGCTGCTCACCACTA | 57799 |
| rs184995059 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:620711 | GATGGGCTCCACCGC[A/G]GGCATCCCAGCCCCC | 57799 |
| rs185461592 | snp | C/T | 0.00243739 | 0.0348246 | intron-variant | RAB40C | GRCh38.p7 | 16:626155 | GCCAGCCCTGAGGTC[C/T]CCGAACCTGGGCTGC | 57799 |
| rs185467534 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RAB40C | GRCh38.p7 | 16:604698 | TCATATATGAGTGTA[C/T]GTTTTAATTTATAAG | 57799 |
| rs185512844 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:589456 | CAGCCGCATCGCCTC[A/G]GCTCGGGCGCGCCTG | 57799 |
| rs185520196 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629147 | AAACCTCACAGACTT[C/T]GAGGACCTGGATGGT | 57799 |
| rs185600275 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:600590 | ACCCCGTCTCTACTA[A/G]AAATTCAAAAATTAG | 57799 |
| rs185609443 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RAB40C | GRCh38.p7 | 16:622632 | CCTGCCTCAGGCTCC[C/T]GAGTAGCTAGAACTA | 57799 |
| rs185640836 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RAB40C | GRCh38.p7 | 16:608367 | AAGGTGAGATTTGGG[C/T]GGGGACACAGCCAAA | 57799 |
| rs185653670 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:604332 | CACTAGCACTAAACT[A/G]TAACACAAATACGCA | 57799 |
| rs185750792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:626435 | GCTCCTTCCTGGTTC[C/T]GGGGCTGGTCCTGCT | 57799 |
| rs185809673 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:625776 | CCCACCTTGACCTCC[A/G]CCCACCTTGACCTCC | 57799 |
| rs185825422 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RAB40C | GRCh38.p7 | 16:621653 | GGGTGCCACAACCCG[C/T]TGGTGGGATGAGTGG | 57799 |
| rs185937358 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594694 | GTTCTAGCTGTGTGT[C/G]TTTAGGTGACTGGAC | 57799 |
| rs185966330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596129 | GGCAGTGCCAGCCAG[A/G]TCTCTCGCAGGGTGG | 57799 |
| rs186103883 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:616730 | TTGGAAATACATTCG[C/T]CTTGGAGAATTCAAC | 57799 |
| rs186423042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:621375 | AGACTAGCAAGGACT[A/G]TCTGTCCCAGCCGGG | 57799 |
| rs186425992 | snp | A/G | 0.029116 | 0.117091 | intron-variant | RAB40C | GRCh38.p7 | 16:598577 | AAAAAAAAAAAAAAA[A/G]AAAGAAAAAAGAAAA | 57799 |
| rs186481072 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RAB40C | GRCh38.p7 | 16:610997 | TGGTATCCATGGGGA[C/T]GTTGTTTCATAGTCT | 57799 |
| rs186528746 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595084 | TCGGGGGTTTTGCTC[A/G]TTTTCTGGGGCAGTG | 57799 |
| rs186534911 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RAB40C | GRCh38.p7 | 16:616173 | AGGCTAGATAATGGC[A/G]TGAACCCGGGAGACG | 57799 |
| rs186596094 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RAB40C | GRCh38.p7 | 16:615957 | ACAGAGTGAGACTCC[A/G]TCTCAAAAAAGAAAA | 57799 |
| rs186659798 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:591927 | CTTCCAGTGGCATGG[C/T]TAAAATACACTAGAT | 57799 |
| rs186663596 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RAB40C | GRCh38.p7 | 16:590963 | GATCTGGGGTCCGGG[A/G]AAAGATGTCATGGTC | 57799 |
| rs186820807 | snp | A/C/T | 0.000107896 | 0.00734414 | synonymous-codon | RAB40C | GRCh38.p7 | 16:627616 | GAGTAACTGCAAGAT[A/C/T]TCCTAGCGGGGATGG | 57799 |
| rs186824698 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | RAB40C | GRCh38.p7 | 16:607386 | TGGGTGCCTGTAATC[C/G]CAGCTACTCGGGAGG | 57799 |
| rs186846668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:605765 | GAGGAGTCTCAGACG[C/T]GTTTGGTCAACACAG | 57799 |
| rs186976196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:611387 | CAAGGAGAAGCAGCT[A/G]TGGCCTTTGTGGCAA | 57799 |
| rs187180719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:591393 | CGGGGAAGGTGTCAC[A/G]GACCCAGGTCTGGTG | 57799 |
| rs187267612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596943 | TCTCGTGCTGAGATC[A/G]GGATTTTGAGTAAAG | 57799 |
| rs187285404 | snp | C/T | 0.00116692 | 0.0241267 | intron-variant | RAB40C | GRCh38.p7 | 16:618274 | AGGTAAGACCAGCAC[C/T]GCTCTTTCCATTGCT | 57799 |
| rs187332299 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RAB40C | GRCh38.p7 | 16:624588 | CTAATTTTCAGATGG[A/G]CAGTGCCCTCTTCTT | 57799 |
| rs187335383 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RAB40C | GRCh38.p7 | 16:602999 | GGAGAATTTTAAGAG[A/G]TAGGGTCTCACTGTG | 57799 |
| rs187394183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:623211 | CTCTCTTTCTAGAGT[C/T]TTCAGTGTCATGCGA | 57799 |
| rs187397097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:601312 | AATGAAAGAGCAGGA[A/G]AAACCGTCTGTGTCC | 57799 |
| rs187399209 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593338 | TATTCTCCTTTGAAA[A/G]AGTTGTAGCAGGAGC | 57799 |
| rs187528011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:623481 | GGTGAAACCCTGTCT[C/T]TACTAAAAAAAAATA | 57799 |
| rs187758573 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | RAB40C | GRCh38.p7 | 16:602572 | TAGCTGGGATTACAG[A/G]CACCTGCCACCACGC | 57799 |
| rs187921437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:618995 | CAGGTCTGGCGGACG[C/T]ACTGGGGCCATGTGT | 57799 |
| rs187925418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:597889 | GCGGAGTGCTGGAGC[C/T]CAGGAGTTTGAGGCC | 57799 |
| rs188057499 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594173 | TCCTGGGAGCAAGTT[C/T]TCCTCCCGCCACGTT | 57799 |
| rs188067332 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:614773 | TCTGCCGCATCCCGA[C/T]GGTGAACTGCCAAAC | 57799 |
| rs188132808 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RAB40C | GRCh38.p7 | 16:613687 | TAAAGTATAATTTCC[A/G]TATTTTTTTCCCCAG | 57799 |
| rs188205189 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RAB40C | GRCh38.p7 | 16:590701 | GGGACGGTGTCACGG[A/G]TCCGGGATCTCAGGG | 57799 |
| rs188226276 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:609739 | AAAAAGCCATAGAAG[A/G]GCTAGAAAAGAAAGT | 57799 |
| rs188267912 | snp | A/C/T | | | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588170 | ACTATCCACCCCCCG[A/C/T]TTCCAGGCAGTCTCA | 57799 |
| rs188299740 | snp | A/C | | | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628369 | ACTCAAAACTCAGAT[A/C]ATCTCGCCCACCCTG | 57799 |
| rs188421563 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RAB40C | GRCh38.p7 | 16:592776 | GTGCTTCTGAGGGCC[A/G]GCTCAGCCATGCTGG | 57799 |
| rs188562552 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:608132 | TTGACTCACAGTTCC[A/G/T]CATGGCTGCAGAGGC | 57799 |
| rs188705340 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RAB40C | GRCh38.p7 | 16:614105 | AACTCTACCGCATCC[C/T]GATGGTGAACTGCCA | 57799 |
| rs188919424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:606072 | GGCCGCAATAGATGG[C/T]CTTTCTACTCCTTTT | 57799 |
| rs188992840 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:598493 | TTGAACCTGGGTGGC[A/G]GAGGTTGCAGAGAGC | 57799 |
| rs188999159 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:620815 | CGACGGGCTCCACCG[C/T]GGGCATCCCAGCCAC | 57799 |
| rs189135848 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594771 | TGACCACTGCAGCCC[A/C]GAGTCCCTTCTCCTC | 57799 |
| rs189142159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:624923 | GTGGCAAAAAGTCCC[C/T]GTGGCAAAACCTGCT | 57799 |
| rs189158418 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RAB40C | GRCh38.p7 | 16:615996 | GGTGCAGTGGCTCAC[A/G]CCTGTAATCCTAGCA | 57799 |
| rs189208247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:626806 | AACCGGGCGTGGTGA[C/T]GCACACCTGTAGTCC | 57799 |
| rs189219278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RAB40C, LOC101929280 | GRCh38.p7 | 16:597992 | TGGCTCACACCTGTA[A/G]TTCCAGCACTTTGGG | 57799 |
| rs189274591 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:621419 | CCTCCCTCCGTTAGA[C/G]AGTGGAGAGGCCTGG | 57799 |
| rs189387288 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:604348 | TAACACAAATACGCA[A/C/T]GAGGCCTTCTGAAGG | 57799 |
| rs189506703 | snp | C/G | 0.0170251 | 0.090679 | intron-variant, upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:589985 | GAGGGCGGGGAAGTC[C/G]TGACGGACGGGCGGG | 57799 |
| rs189515625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:620420 | GAGCTGTGTGGGTGA[C/T]TTACATCTACAAAAA | 57799 |
| rs189785109 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:615022 | TTTGGCACAACCATT[C/G]TTCCTTCTTGTCTTG | 57799 |
| rs189801516 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | RAB40C | GRCh38.p7 | 16:616219 | AGAGATCGCACCACT[G/T]CACTCCAGCCTGGGT | 57799 |
| rs189805505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595754 | ATTACAGCCACCTGC[C/T]ACCACACCCAGCTAA | 57799 |
| rs189814358 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:606818 | TCAGCCAGGAAAGGC[A/G]GTTAAGGACTTATGT | 57799 |
| rs189927988 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RAB40C | GRCh38.p7 | 16:626184 | GCCCTGATCACATGG[A/G]GGCTGAGGGGGGCCA | 57799 |
| rs189930249 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:605407 | TTAAAGTCTGCAATA[A/C]AGTGAGTGCGGACAG | 57799 |
| rs189939891 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:592229 | CTGACTGCCCTGAGC[A/G]TCTGCTATTTGCTGA | 57799 |
| rs189949121 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:613168 | GCCCTGGCCTGTAGA[A/G]TCAAGAGCAGGGACA | 57799 |
| rs190043584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594479 | GGGCACCCTGTGTGG[A/G]TGTCCCAGCTTCTTC | 57799 |
| rs190049108 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:604216 | TGTACCACCACACCC[A/G]GCTCAGAGCTAGTTC | 57799 |
| rs190445742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:599117 | CACAAACACAGTGAC[A/G]CTGATCAGGGTTGCC | 57799 |
| rs190463874 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:622672 | CACCGCGTCCAGCTA[A/C]TTTTTGTATTTTTAG | 57799 |
| rs190581720 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:608449 | TGATCCTGAAGGGCT[A/G]GGTGCTGTGCCAAAC | 57799 |
| rs190760040 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:626807 | ACCGGGCGTGGTGAC[A/G]CACACCTGTAGTCCC | 57799 |
| rs190825984 | snp | C/T | 0.000819874 | 0.0202303 | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629693 | GGGGGTGTGGACGCC[C/T]CGGAGGTCACAGCTG | 57799 |
| rs190854629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:600424 | TGTCACCTAACCTGC[C/T]GAGTTTAAAACATTG | 57799 |
| rs190857461 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | RAB40C | GRCh38.p7 | 16:591544 | TAGAAGAAAATACCT[C/G]TGTAATGAGTTACTG | 57799 |
| rs191126454 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:622199 | AGCAGTTCTACTTCT[A/G]GGAATTTATCGTGTA | 57799 |
| rs191259402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596191 | GTGTTGTGGCCTGCA[C/T]GATGAGCTAAATTGA | 57799 |
| rs191420511 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:614915 | GAACTGCCTAACTCT[A/G]CCGCATCCTGATGAA | 57799 |
| rs191525090 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:591174 | TCTGGGATCTCAGGG[A/G]AAGGTGTCATGGGCC | 57799 |
| rs191647629 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587719 | GGCTGGGTCTGGAGA[A/G]CGTTTTACTTTGTTT | 57799 |
| rs191660861 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:607869 | GAAAACGAAGTCGCA[A/C]CTAGTAAAGCAAACG | 57799 |
| rs191668458 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:627980 | TTCAGGGAAGCCTGG[A/G]TGTGGCCCGGTGGTG | 57799 |
| rs191679925 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RAB40C | GRCh38.p7 | 16:605800 | CCATTGCTGTTGGGA[C/T]GTACTGAGGAGTGGA | 57799 |
| rs191779521 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:611191 | TCTGTGGGTGGGTGA[C/T]GTGGTCCCCAGGCTT | 57799 |
| rs191785753 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RAB40C | GRCh38.p7 | 16:624847 | ACTGTCACTGCCGAG[A/G]TATTTAGGGCAGGTG | 57799 |
| rs191787778 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RAB40C | GRCh38.p7 | 16:603768 | GCCCCTCAGGCCCTG[C/T]CGAGTCAGCCCCCAG | 57799 |
| rs191839692 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:623327 | CTTCTTCAGTGTAAT[A/G]TGTTGTGTGTTCATA | 57799 |
| rs191989149 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:626655 | CTTAAGAGGAAGCAC[A/G]GGCCTGGCACGGTGG | 57799 |
| rs192206536 | snp | C/G | | | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:597410 | GGTGATGTGGTCCTG[C/G]CTGTGTAAACTGACC | 57799 |
| rs192216468 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RAB40C | GRCh38.p7 | 16:618499 | GGTTCAAGCGATTCT[C/T]CTGCCTCAGCCTCCC | 57799 |
| rs192312584 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | RAB40C, LOC101929280 | GRCh38.p7 | 16:597969 | AAAAAAAAAAAGGCC[A/G]GGTGCAGTGGCTCAC | 57799 |
| rs192350094 | snp | C/G | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593416 | TGCTTTCTCTCCTTT[C/G]TTGGGAGGTGCCCTC | 57799 |
| rs192369060 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RAB40C | GRCh38.p7 | 16:614129 | ACTGCCAAACTCTAC[C/T]GCATCCCGATGGTGA | 57799 |
| rs192437002 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RAB40C | GRCh38.p7 | 16:602638 | AGGTTTCACCATGTC[A/G]GCCAGGCTGGTCTCG | 57799 |
| rs192608767 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | RAB40C | GRCh38.p7 | 16:620526 | AAAATATGGGGCGCA[G/T]TTATGTTGGATGACA | 57799 |
| rs192711471 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:619923 | AGGGCGGGCTGGGTC[A/G]CACCCTGTCCTGGGA | 57799 |
| rs192777795 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:623987 | TGCGTTCTTACCTCA[C/G]CTGGGTTGCACATCT | 57799 |
| rs192788662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594252 | TCCTGGCTTGACTTT[A/G]TTTCTCTCTCTGCTC | 57799 |
| rs192846335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RAB40C, LOC101929280 | GRCh38.p7 | 16:598100 | AAATACAAAAATTGG[C/T]CAGGCATGGTGGCTC | 57799 |
| rs192896549 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593107 | AGGAAGCGCCTCTGG[A/G]CTGTGGAACGCGCTT | 57799 |
| rs192967607 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:608327 | ATCTCCATCTGGCCC[C/G]GCCCTCAACCTGTGG | 57799 |
| rs193128788 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RAB40C | GRCh38.p7 | 16:613830 | GGTGGGGGTCGTGGG[C/T]AGCACCCAGGTCTAG | 57799 |
| rs193187824 | snp | A/G | 0.00438332 | 0.0466095 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588827 | TAACAGCGCTACTGA[A/G]CGCAGAGCACGTATC | 57799 |
| rs193191746 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628508 | GGGGTCCCCACAGCT[A/G]CAGCTCTCCTGTGAG | 57799 |
| rs193215763 | snp | A/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:601665 | GGAATGCTTATAAGT[A/T]TATCAAATAGTAAAA | 57799 |
| rs199630964 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:616633 | GTGAGCCACCGCGCC[C/T]GGCCAGAAGCAGCAT | 57799 |
| rs199642487 | in-del | -/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:612281 | GTAGAATCAAGAGCA[-/C]GGGACAGCCGCCCTG | 57799 |
| rs199667109 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628531 | CCTGTGAGGTTGCAC[A/G]GCATCAGAACCATCC | 57799 |
| rs199734843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595443 | ACCTGGGCCTGGGGA[C/T]GGCTGCCACACACCT | 57799 |
| rs199735737 | in-del | -/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:612042 | GTAGAATCAAGAGCA[-/C]GGGACAGCCGCCCTG | 57799 |
| rs199749680 | snp | A/G | 0.000282155 | 0.0118743 | intron-variant | RAB40C | GRCh38.p7 | 16:617189 | GCGCGTCCCCTCAGC[A/G]CCCTGTGCTTCCTCG | 57799 |
| rs199762675 | snp | A/G | 0.000235207 | 0.010842 | intron-variant | RAB40C | GRCh38.p7 | 16:625397 | CTGGCCATGCGTGTC[A/G]GTGACCCCTGATGAC | 57799 |
| rs199820805 | snp | A/G | 0.00016573 | 0.00910152 | missense | RAB40C | GRCh38.p7 | 16:626043 | CTGTGCAACTTCAAC[A/G]TCATCGAGTCCTTCA | 57799 |
| rs199828258 | in-del | -/A | | | intron-variant | RAB40C | GRCh38.p7 | 16:620391 | GTGAAACTCCATCTC[-/A]AAAAAAAAAGGAGGA | 57799 |
| rs199977879 | in-del | -/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:617624 | GAGGCAGGAGGATCA[-/C]CTGAGGTCAGGAGTC | 57799 |
| rs199989400 | snp | A/G | 0.000268467 | 0.0115828 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:627640 | GGGATGGGCGGGGCC[A/G]CCTGTGCAGATGCCA | 57799 |
| rs200028275 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:623024 | CGCCGGAGCAAGCCT[A/C]CGGGTCCTCCTGTGC | 57799 |
| rs200056758 | in-del | -/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:613348 | GAATCAAGAGCAGGG[-/G]ACAGCTGCCCTCGTC | 57799 |
| rs200130873 | in-del | -/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:612557 | GTAGAATCAAGAGCA[-/C]GGGACAGCCGCCCTG | 57799 |
| rs200136711 | snp | A/G | 0.00297678 | 0.0384646 | synonymous-codon | RAB40C | GRCh38.p7 | 16:590333 | GAGCTACGACTACCT[A/G]CTCAAGTTCCTGCTG | 57799 |
| rs200206306 | in-del | -/GGCCTGTA | | | intron-variant | RAB40C | GRCh38.p7 | 16:611746 | AGGGACAGCCGCCCT[-/GGCCTGTA]GATTCAAGAGCAGGG | 57799 |
| rs200209367 | snp | A/G | 0.000182118 | 0.00954074 | intron-variant | RAB40C | GRCh38.p7 | 16:617204 | GCCCTGTGCTTCCTC[A/G]CAGGGATCGACTACA | 57799 |
| rs200244078 | snp | G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:602268 | TTTTTTTTTGGTTTT[G/T]TTTTTTTTTATTAGA | 57799 |
| rs200311389 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:591694 | CCTCCTGGGTTCAAG[C/T]GATTCCCCTGTCTCA | 57799 |
| rs200362787 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:604061 | TTCTTTTTTCTTTTT[C/T]TTTTTTTTTTTTTTG | 57799 |
| rs200393855 | snp | C/T | 5.01282e-05 | 0.00500616 | intron-variant | RAB40C | GRCh38.p7 | 16:618283 | CAGCACCGCTCTTTC[C/T]ATTGCTTTTCAAAGG | 57799 |
| rs200405053 | in-del | -/GC | 0.0115144 | 0.0749975 | intron-variant | RAB40C | GRCh38.p7 | 16:622471 | CCTAGAGCAGGGCGA[-/GC]GCGCGTCCTGACTCA | 57799 |
| rs200643692 | in-del | -/CCTG | | | intron-variant | RAB40C | GRCh38.p7 | 16:612643 | GGACAGCCGCCTTTG[-/CCTG]TAGAATCAAGAGCAG | 57799 |
| rs200704206 | in-del | -/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:612111 | GTAGAATCAAGAGCA[-/C]GGGACAGCCGCCCTG | 57799 |
| rs200719024 | snp | A/G | 5.02559e-05 | 0.00501253 | synonymous-codon | RAB40C | GRCh38.p7 | 16:618206 | ATGTTTCAGGGACAC[A/G]TCGGGCCAGGGCCGG | 57799 |
| rs200782060 | snp | A/C/T | 3.44305e-05 | 0.00414898 | missense | RAB40C | GRCh38.p7 | 16:627581 | CGTCCACCCCAGAGC[A/C/T]CCCCCCAGAACTGCT | 57799 |
| rs200787887 | snp | A/C | 0.0117466 | 0.075732 | synonymous-codon | RAB40C | GRCh38.p7 | 16:590408 | GCAGGACGGCGCGGC[A/C]GAGTCCCCGTACGCC | 57799 |
| rs200805464 | snp | C/G | | | synonymous-codon, intron-variant | RAB40C | GRCh38.p7 | 16:625919 | ACCCGGAGTCCCCCG[C/G]ATCTTGGTTGGAAAC | 57799 |
| rs200919878 | in-del | -/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:612452 | GTAGAATCAAGAGCA[-/C]GGGACAGCCGCCCTG | 57799 |
| rs201052399 | in-del | -/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:612247 | GTAGAATCAAGAGCA[-/C]GGGACAGCCGCCCTG | 57799 |
| rs201052771 | snp | A/C/G | 0.000405518 | 0.0142339 | intron-variant | RAB40C | GRCh38.p7 | 16:618173 | AGGGACCACAGTCCC[A/C/G]GCCCCTCCCCTCCCC | 57799 |
| rs201108714 | snp | C/T | 0.00030011 | 0.012246 | intron-variant | RAB40C | GRCh38.p7 | 16:617175 | TCGCTCCAGGAGTGG[C/T]GCGTCCCCTCAGCGC | 57799 |
| rs201121584 | in-del | -/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:611864 | GGCCTGTAGAATCAA[-/G]AGCACGGGACAGCCG | 57799 |
| rs201158627 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:621920 | CGGCACACAGGTGGG[C/T]GGGTGGATGTGAGTG | 57799 |
| rs201194057 | in-del | -/CT | | | intron-variant | RAB40C | GRCh38.p7 | 16:614152 | ATGGTGAACTGCTAA[-/CT]CTACCGCATCCCGAT | 57799 |
| rs201370882 | snp | C/T | 0.000119447 | 0.00772717 | intron-variant | RAB40C | GRCh38.p7 | 16:625536 | TCCGGGGAGCCCTCC[C/T]GGGGAAGGCAGGCTG | 57799 |
| rs201535632 | snp | G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:604076 | CTTTTTTTTTTTTTT[G/T]AGACTCTCGTTCTGT | 57799 |
| rs201703817 | in-del | -/A | | | intron-variant | RAB40C | GRCh38.p7 | 16:613309 | TGTAGAATCAAGAGC[-/A]AGGGACAGCCGCCCT | 57799 |
| rs201729155 | in-del | -/TC | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594823 | CTCGTCTTCCTTTTT[-/TC]TTTTTTTTTTTTTTT | 57799 |
| rs201729621 | snp | A/G | 3.47017e-05 | 0.00416529 | synonymous-codon | RAB40C | GRCh38.p7 | 16:590339 | CGACTACCTGCTCAA[A/G]TTCCTGCTGGTGGGC | 57799 |
| rs201755228 | in-del | -/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:612487 | GTAGAATCAAGAGCA[-/C]GGGACAGCCGCCCTG | 57799 |
| rs201836577 | snp | A/G | 1.66103e-05 | 0.00288182 | missense | RAB40C | GRCh38.p7 | 16:627528 | GGGCCGGGGGCGGCG[A/G]CAGCAAGGGCAACAG | 57799 |
| rs201851102 | snp | C/G | 0.000975408 | 0.0220625 | intron-variant | RAB40C | GRCh38.p7 | 16:617317 | TGAGGACACAAATGC[C/G]GAAGGGAGAACAGAA | 57799 |
| rs201859512 | snp | C/T | | | intron-variant, downstream-variant-500B | RAB40C, LOC101929280 | GRCh38.p7 | 16:597968 | AAAAAAAAAAAAGGC[C/T]GGGTGCAGTGGCTCA | 57799 |
| rs201886226 | snp | C/G/T | 0.00199481 | 0.0315187 | intron-variant | RAB40C | GRCh38.p7 | 16:624006 | GGTTGCACATCTCTC[C/G/T]TTGGCCAGCATGCAC | 57799 |
| rs202058589 | in-del | -/A | | | intron-variant | RAB40C | GRCh38.p7 | 16:599612 | AGTCAGCGTGGATTC[-/A]GCAAGGTTTTGTTAC | 57799 |
| rs202063822 | in-del | -/C | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629335 | TGCCAGGGGCCAGTG[-/C]TGCTTCATACCCGGC | 57799 |
| rs202115814 | snp | G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:602262 | TGTTTTTTTTTTTTT[G/T]GTTTTGTTTTTTTTT | 57799 |
| rs202230568 | snp | G/T | 1.94098e-05 | 0.0031152 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:627652 | GCCGCCTGTGCAGAT[G/T]CCAGGAGGGCTCGAG | 57799 |
| rs367544212 | snp | A/G | | | synonymous-codon | RAB40C | GRCh38.p7 | 16:617260 | CCGGCGCGTGAAGCT[A/G]GAGCTCTGGTGAGTT | 57799 |
| rs367555419 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594088 | AGCCCAGCCGCTCCC[C/G]CTCTGCAGGGGGCAT | 57799 |
| rs367608832 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:601253 | TCAAGGCTGTATCAC[C/T]GAGTATCTGCTCATT | 57799 |
| rs367612369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:614344 | GCTAACTCTGCCGCA[C/T]CCCGATGGTGAACTG | 57799 |
| rs367613720 | snp | C/T | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593980 | GCTGCAGTTCAGGAG[C/T]GAACCTGCAGTCAGG | 57799 |
| rs367616611 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | RAB40C | GRCh38.p7 | 16:607972 | CTGAAGGGTGCCTGA[C/G]TCTGCAGCCAGGCAA | 57799 |
| rs367710808 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:604720 | ATTTATAAGCTTGCC[C/T]AGCCTGGGCAACATA | 57799 |
| rs367731044 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:622381 | CCCTTGACCCCGCCC[A/G]CGAGGCATGAGCGGC | 57799 |
| rs367961112 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:620145 | CACGCCTGTAATCCC[A/T]GCACTTTGGGAGGCC | 57799 |
| rs368099707 | snp | C/T | | | intron-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595606 | AACTTTTTTCTTCTT[C/T]TTTTTTTTTTTTTTG | 57799 |
| rs368101804 | snp | A/G | | | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596741 | GAAGGACTGGCTGCC[A/G]AGACCATGGGCTGTG | 57799 |
| rs368119235 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:611552 | GTTGACGGCCTGAGC[A/G]CGGTGCCTCCCTGAA | 57799 |
| rs368123941 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:622159 | GTAAAAAATGATAGC[A/C/G]AAAAGGACACCCACT | 57799 |
| rs368232575 | snp | C/T | 0.000153988 | 0.00877328 | missense | RAB40C | GRCh38.p7 | 16:625980 | CCGACGGAGCAGGCC[C/T]GCGCGTACGCAGAGA | 57799 |
| rs368280779 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RAB40C | GRCh38.p7 | 16:612945 | AGAGCACGGGACAGC[C/T]GCCCTGGCCTGTAGA | 57799 |
| rs368285177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593448 | GTGTTTCCAGCTTCC[A/G]TGTTTCTTCAGGGCT | 57799 |
| rs368288404 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:622563 | GCCAGGCTGGAGTGC[A/C/T]GTGGCGCGATCTCGG | 57799 |
| rs368389504 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:614556 | CCTAAACCTCGTCCC[A/G]ATGGTGAACTGCCTA | 57799 |
| rs368501505 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RAB40C | GRCh38.p7 | 16:619259 | TGGGGCCATGTGTGC[A/G]GTGTGTGTGCAGGTG | 57799 |
| rs368503544 | snp | A/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:602159 | GGCACATTTAATGAT[A/T]ATTCAATGAAGTGTA | 57799 |
| rs368725618 | snp | C/G/T | 0.000306318 | 0.0123721 | intron-variant | RAB40C | GRCh38.p7 | 16:618188 | GGCCCCTCCCCTCCC[C/G/T]GTATGTTTCAGGGAC | 57799 |
| rs368764890 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:590736 | GTGTCATGGGTCCGG[A/G]ATCTGGAGCCCAGGG | 57799 |
| rs368834371 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:591743 | ACTACAGGTGTATGC[C/T]ACCACGCCCGGCTAA | 57799 |
| rs368847759 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:617456 | TCTGGGACACTGTGT[C/G]CCTAGAGATCGCGGC | 57799 |
| rs368857770 | snp | C/G | | | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628722 | CTCCTCCACCCAGTG[C/G]TTCTGCCCATGCCTG | 57799 |
| rs368899026 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:610171 | AGCAGCCGAGGCGCC[A/G]GTGGCTTTGCTCTGG | 57799 |
| rs368904907 | snp | G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:617893 | CAGCGTTGATGAGAC[G/T]TGAATGTCCACAGGG | 57799 |
| rs369008599 | snp | A/G | 1.65441e-05 | 0.00287607 | missense | RAB40C | GRCh38.p7 | 16:617213 | TTCCTCGCAGGGATC[A/G]ACTACAAGACCACCA | 57799 |
| rs369044756 | snp | G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:616368 | ATTTATTTATTTATT[G/T]AGTACTGTCACCCAG | 57799 |
| rs369049465 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RAB40C | GRCh38.p7 | 16:614035 | GAACTGCCTAACTCT[A/G]CCGCGTCCCGATGGT | 57799 |
| rs369297463 | in-del | -/CGAACTCTACCGCATCCCTATGGTGAACTGC | | | intron-variant | RAB40C | GRCh38.p7 | 16:614178 | CCGATGGTGAACTGC[lengthTooLong]TAACTCTGCCGCATC | 57799 |
| rs369325187 | snp | C/T | 0.0781911 | 0.181609 | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629479 | GGGCCTGGTCACGGC[C/T]ATTCTCCTCTTCCCG | 57799 |
| rs369368447 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | RAB40C | GRCh38.p7 | 16:613389 | AGAGCAGGGACTGCC[A/G]CCCTCGCCTGTAGAA | 57799 |
| rs369430036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:599466 | CTTCCCTTGGGGCCA[C/T]GCCGTGCCTCCTCCG | 57799 |
| rs369536775 | snp | C/T | | | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:597836 | CTGGGCACGGTGGCT[C/T]ACACCTGCAATCTCA | 57799 |
| rs369580907 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:609480 | GAAGCGGCCACGAGA[C/T]GCCGCCGAGAGCCCC | 57799 |
| rs369584664 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:620816 | GACGGGCTCCACCGC[A/G]GGCATCCCAGCCACC | 57799 |
| rs369585698 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | RAB40C | GRCh38.p7 | 16:618163 | AGCCTCTCACAGGGA[C/T]CACAGTCCCGGCCCC | 57799 |
| rs369597956 | snp | C/T | 8.31926e-05 | 0.00644898 | synonymous-codon | RAB40C | GRCh38.p7 | 16:618254 | GTCCTACTCCAGGGG[C/T]GCTCAGGTAAGACCA | 57799 |
| rs369599088 | snp | A/G | 3.47228e-05 | 0.00416656 | intron-variant | RAB40C | GRCh38.p7 | 16:626166 | GGTCCCCGAACCTGG[A/G]CTGCCCTGATCACAT | 57799 |
| rs369620762 | snp | C/G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:617767 | AGAATCACTTGAACC[C/G/T]GGGAGGCAGAAGTTG | 57799 |
| rs369707215 | snp | G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:592302 | CCACTCTCTCAACTC[G/T]GGGGTTGGCAGAGCG | 57799 |
| rs369788859 | in-del | -/GGGGACAGGGTGGCA | 0.00318978 | 0.0398085 | intron-variant | RAB40C | GRCh38.p7 | 16:609340 | CCACTGGGGATGGTG[-/GGGGACAGGGTGGCA]GGGGACAGGGTGGCC | 57799 |
| rs369801150 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:608024 | TCCCTCCACACGTTC[C/T]TGGGCAGCCTCCACG | 57799 |
| rs370023212 | snp | C/G | 1.66988e-05 | 0.00288949 | intron-variant | RAB40C | GRCh38.p7 | 16:625428 | CCCCAAGTCTCTGTT[C/G]CAGGGGATCCTCTTG | 57799 |
| rs370044568 | snp | C/T | 4.95749e-05 | 0.00497845 | intron-variant | RAB40C | GRCh38.p7 | 16:617281 | CTGGTGAGTTGGGGC[C/T]GCGGCACTTCAGTTC | 57799 |
| rs370105709 | snp | A/G | | | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:589270 | ACGGTGCGCCCCGCC[A/G]CCGCCGGGCGGAAGT | 57799 |
| rs370110148 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:604445 | GGTGTTTCTCTAGAA[C/T]ATATGTGAGTCCTTC | 57799 |
| rs370110769 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:603696 | TGGCACATATATGTA[C/T]CTATGCAGCCAGTAC | 57799 |
| rs370201342 | snp | G/T | 1.75336e-05 | 0.00296082 | intron-variant | RAB40C | GRCh38.p7 | 16:627316 | CCCCCACAGCCCCAT[G/T]GTCTGACACCCCCTC | 57799 |
| rs370206056 | snp | C/T | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593042 | CGTGCTCTCAGGGCC[C/T]GGGGCACACTTCCAG | 57799 |
| rs370219696 | snp | G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:618734 | TGTGTGTGCAGGCAT[G/T]TGCACAGGTCTGGCG | 57799 |
| rs370234444 | snp | G/T | 1.67097e-05 | 0.00289043 | intron-variant | RAB40C | GRCh38.p7 | 16:618287 | ACCGCTCTTTCCATT[G/T]CTTTTCAAAGGATGT | 57799 |
| rs370287052 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:622279 | ACCGTTACCCAAGAG[C/T]TGGCGCAGTACCAGT | 57799 |
| rs370444305 | snp | A/G | 6.62866e-05 | 0.00575664 | missense | RAB40C | GRCh38.p7 | 16:627518 | CTGGCCAGCGGGGCC[A/G]GGGGCGGCGGCAGCA | 57799 |
| rs370505779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:624170 | ATCCTCAGTTACTTC[C/T]GAGTTGTGGGCTTGC | 57799 |
| rs370535109 | snp | G/T | 4.99988e-05 | 0.00499969 | intron-variant | RAB40C | GRCh38.p7 | 16:618270 | GCTCAGGTAAGACCA[G/T]CACCGCTCTTTCCAT | 57799 |
| rs370585823 | snp | C/G | 1.75087e-05 | 0.00295872 | missense | RAB40C | GRCh38.p7 | 16:590382 | GGCAAGGGCGAGATC[C/G]TGGAGAGCCTGCAGG | 57799 |
| rs370761277 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:597765 | AAGTTGGTGGAATTA[C/T]AGGCATGAGCCACTG | 57799 |
| rs370819515 | in-del | -/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:607020 | ACCTGAGCCAAGGAA[-/C]CCTCCACTCAGGTGG | 57799 |
| rs370819829 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588472 | GTAGAGGCTGCAGTG[A/G]GCCGAGATCGCGCTA | 57799 |
| rs370909308 | snp | A/T | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:590087 | CGGCGGCCCTGGTGG[A/T]GCGGGAAGCGGCGGG | 57799 |
| rs370913500 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:605115 | TAATAGTCTTAGCTA[C/T]TCAGGAGGCTGAGGC | 57799 |
| rs370944568 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:614218 | AACTGCTAACTCTGC[C/T]GCATCCCGATGGTGA | 57799 |
| rs371073143 | snp | A/G | 1.69732e-05 | 0.00291313 | intron-variant | RAB40C | GRCh38.p7 | 16:625529 | GCCTGGGTCCGGGGA[A/G]CCCTCCCGGGGAAGG | 57799 |
| rs371233255 | snp | A/G | 1.98742e-05 | 0.00315225 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:627665 | ATGCCAGGAGGGCTC[A/G]AGCTGGACACTCCTG | 57799 |
| rs371287321 | snp | C/T | 0.000171541 | 0.00925966 | intron-variant | RAB40C | GRCh38.p7 | 16:590445 | AACGGTAAGGCCCGG[C/T]CCGCGGCGCGCGCTG | 57799 |
| rs371340284 | in-del | -/GCCGAGATTGTGCCATTGCACGCCAACCTGGGCGA | | | intron-variant | RAB40C | GRCh38.p7 | 16:620339 | TGGAGGTTGCAGTGA[lengthTooLong]CGAGTGAAACTCCAT | 57799 |
| rs371383114 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:611644 | AGGGACAGCCGCCCT[A/G]GCCTGTAGAATCAAG | 57799 |
| rs371465113 | snp | C/G | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594650 | CGTCGGCTGCTTATC[C/G]CCAGGGCTAGCTGAG | 57799 |
| rs371615491 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:624844 | ATGACTGTCACTGCC[A/G]AGATATTTAGGGCAG | 57799 |
| rs371649263 | in-del | -/GT | | | intron-variant | RAB40C | GRCh38.p7 | 16:601814 | TCCCTGCAAAAAAAA[-/GT]AAAAAAAAAAAAAAA | 57799 |
| rs371653841 | snp | A/G | 0.000134957 | 0.00821343 | intron-variant | RAB40C | GRCh38.p7 | 16:626132 | CCGAGGTGGGTGGGC[A/G]GGCGCCGGCCAGCCC | 57799 |
| rs371710152 | snp | G/T | | | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628402 | GAGTGCAGAGCTATC[G/T]GTAGACTTAGGAATA | 57799 |
| rs371750074 | snp | C/T | 0.000430428 | 0.0146639 | intron-variant | RAB40C | GRCh38.p7 | 16:617203 | CGCCCTGTGCTTCCT[C/T]GCAGGGATCGACTAC | 57799 |
| rs371877783 | in-del | -/C | | | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587687 | AGGAGGTGGGAACTA[-/C]GGCAGCAGTGGCCCA | 57799 |
| rs371885916 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593519 | CTGTGCAAGGCTTAC[C/T]GCTTCAGCATGGCCC | 57799 |
| rs371890595 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:608145 | CCGCATGGCTGCAGA[C/G]GCCTCAGGAAATTTA | 57799 |
| rs371914210 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:601893 | AGCACTTTGGGAGGC[C/T]GAGGTGGGTGGATCA | 57799 |
| rs371922193 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:607747 | AGTGAGCCGAGATCG[C/T]GCCACTGCACTCCAG | 57799 |
| rs371999985 | snp | C/T | 0.000317348 | 0.0125926 | intron-variant | RAB40C | GRCh38.p7 | 16:618172 | CAGGGACCACAGTCC[C/T]GGCCCCTCCCCTCCC | 57799 |
| rs372048858 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:601572 | TAGTCTCAGTCAGTT[C/T]ACTAGGGCCATGCAT | 57799 |
| rs372061674 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:617343 | CAGAACCCTTAGAGA[A/G]ACAGGAAGGCGTCCT | 57799 |
| rs372126150 | snp | C/T | 8.32702e-05 | 0.00645199 | synonymous-codon | RAB40C | GRCh38.p7 | 16:625988 | GCAGGCCCGCGCGTA[C/T]GCAGAGAAGAACTGC | 57799 |
| rs372182834 | snp | C/G | | | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:597435 | CTGACCCTGATGAAA[C/G]ACATGCCCATCCTGT | 57799 |
| rs372187993 | snp | A/G | 0.000480694 | 0.0154957 | intron-variant | RAB40C | GRCh38.p7 | 16:617194 | TCCCCTCAGCGCCCT[A/G]TGCTTCCTCGCAGGG | 57799 |
| rs372289465 | snp | A/G | 1.65364e-05 | 0.0028754 | intron-variant | RAB40C | GRCh38.p7 | 16:617315 | GGTGAGGACACAAAT[A/G]CCGAAGGGAGAACAG | 57799 |
| rs372440020 | snp | C/T | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594792 | CCTTCTCCTCCCCTG[C/T]ACTTGATTAGGTTTT | 57799 |
| rs372502055 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:621153 | CCTGGGTTGAGGGTG[C/T]CAGGTGCTTCCTTGC | 57799 |
| rs372538109 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:605385 | ATTTGTGTACAAAAA[A/G]ACCCCTTTAAAGTCT | 57799 |
| rs372552772 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:627805 | CCAAGCGCGGCAGGC[A/G]GGAGGAGGGGGCGCG | 57799 |
| rs372663275 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:612433 | AGGGACAGCCGCCTT[C/T]GCCTGTAGAATCAAG | 57799 |
| rs372706262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:621343 | CAGGGTTTCTCCCGC[C/T]GCCCCTGATGAGACA | 57799 |
| rs372711770 | snp | A/C | | | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:597937 | GAGACCCCATCTCTA[A/C]AAAAAAAAAAAAAAA | 57799 |
| rs372748948 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595671 | GCAGTGGCACGGTCT[C/T]GGCTCACTGCAAGCT | 57799 |